Ignite Creation Date:
2024-05-05 @ 5:03 PM
Last Modification Date:
2024-10-26 @ 9:27 AM
Study NCT ID:
NCT00371046
Status:
COMPLETED
Last Update Posted:
2007-03-02
First Post:
2006-08-31
Brief Title:
Does Fetal Fibronectin and Ultrasound Cervical Length Help in the Evaluation of Women With Suspected Preterm Labor
Sponsor:
Thomas Jefferson University
Organization:
Thomas Jefferson University
Study Overview
Official Title:
The Use of Fetal Fibronectin and Transvaginal Ultrasound Cervical Length in Women With Threatened Preterm LaborA Randomized Trial
Status:
COMPLETED
Status Verified Date:
2007-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The objective of this study is to investigate the effect of the use of both sonographic cervical length CL and fetal fibronectin FFN on the length of outpatient triage and preterm labor interventions in symptomatic women with intact membranes
We performed a randomized trial of the use of transvaginal ultrasound cervical length and fetal fibronectin in women being evaluated for suspected PTL at a gestational age between 24 and 33 weeks 6 days Women are randomized to either a standard blinded or a protocol arm Women in the standard arm are evaluated without the results of the CL and FFN while women in the protocol arm are evaluated using the results of the CL and FFN and managing physicians are asked to follow a specific PTL algorithm to determine a womens eligibility for treatment The primary outcome is length of stay in the triage area before discharge
We performed a randomized trial of the use of transvaginal ultrasound cervical length and fetal fibronectin in women being evaluated for suspected PTL at a gestational age between 24 and 33 weeks 6 days Women are randomized to either a standard blinded or a protocol arm Women in the standard arm are evaluated without the results of the CL and FFN while women in the protocol arm are evaluated using the results of the CL and FFN and managing physicians are asked to follow a specific PTL algorithm to determine a womens eligibility for treatment The primary outcome is length of stay in the triage area before discharge
Detailed Description:
Patients presenting with signs and symptoms suggestive of preterm labor PTL represent a clinical challenge Many studies have shown that over 70 of women evaluated for PTL do not deliver within 7 days and almost 40 of women whether they are treated or not deliver at term On the other hand about 20 of women who are not thought to be in PTL will deliver preterm Women who are diagnosed with PTL are exposed to a variety of evidenced and non-evidenced based interventions including hospital admission tocolysis antenatal steroids maternal transfer and bedrest These interventions are associated with both maternal risks and increased health care costs and often have harmful social financial and psychological effects on the mother as well her family Therefore methods to accurately evaluate the risks of preterm delivery in symptomatic women would help to identify those who would most benefit from standard clinical interventions and help reduce their use in those women who would not deliver preterm A number of retrospective and cohort studies have demonstrated that the use of fetal fibronectin FFN and transvaginal sonographic cervical length TVU CL improves prediction over standard digital exams and that the combination of the two adds prognostic information in women admitted for PTL
The objective of this study was to investigate the effect of the use of both sonographic cervical length and fetal fibronectin on the length of outpatient triage and preterm labor interventions in symptomatic women with intact membranes
Methods
Study design This is a randomized trial of the use of transvaginal ultrasound cervical length and fetal fibronectin in women being evaluated for suspected PTL on labor and delivery at the Thomas Jefferson University Hospital Philadelphia between November 2004 and April 2006 The study was approved by the Internal Review Board
Gestational age was assigned by last menstrual period and first or early second trimester ultrasound If the last menstrual period was unknown or there was a discrepancy regarding the dates the ultrasound dating was used Eligible women who agreed to participate in the study were randomized to either a standard or a protocol arm At the time this study was initiated neither FFN nor CL were routinely used in the management of symptomatic women presenting to LD to be evaluated for PTL Women in the standard arm were evaluated without the results of the CL and FFN while women in the protocol arm were evaluated using the of the CL and FFN and managing physicians were asked to follow a specific PTL algorithm to determine a womens eligibility for treatment Physicians were encouraged to manage protocol patients according to the study recommended protocol for the use of FFN and CL which was reviewed with them for each patient on labor and delivery by a study investigator Once eligible for treatment the management of PTL was then left to the discretion of the physician
Definitions and study procedures
Before randomization all patients being evaluated for preterm labor were monitored in the triage area and uterine activity and fetal heart rate evaluated A speculum exam was performed to rule out ruptured membranes and to obtain a specimen for fetal fibronectin Specimens for fetal fibronectin were obtained with a Dacron swab from the posterior vaginal fornix and placed in buffer which then held on labor and delivery until the patient was either randomized determined to be ineligible or declined to participate in the study After randomization the specimen was immediately analyzed in our in house laboratory Samples were delivered to the laboratory within 1 hour of obtaining the sample and results were available within 1 hour Samples containing 50 ng or more per milliliter were designated as positive The FFN was delayed for 24-36 hours as needed if the patient had intercourse a pelvic exam or a transvaginal ultrasound within 24 hours A digital exam was then performed to determine dilatation and effacement of the cervix
Results of the fibronectin analysis were labeled by one of the study investigators after randomization so that only results from non-blinded specimens would be available to the managing physicians
Randomization was performed by means of computer generated random blocks of numbered sealed opaque envelops which were stratified in two groups based on gestational age 28 weeks and 28 weeks Each envelope was opened sequentially within each strata by one of the study investigators
Following randomization transvaginal ultrasound assessment of the cervix was performed Measurements were obtained using a 5-75 Mhz transvaginal probe placed in the anterior fornix after emptying the bladder The transducer was oriented to obtain a sagittal view of the cervix with the long axis view of the echogenic endocervical mucosa along the length of the canal The probe was withdrawn slightly until the image was blurred and enough pressure then reapplied to restore the image CL was measured from the internal to the external os along the endocervical canal At least three measurements were recorded over 5 minutes and the shortest best measurement in millimeters was used for the study
Using a two-sided t-test with alpha of 005 we calculated that a sample size of 45 patients in each group would have an 80 power to detect a 1 hour 33 in the mean time on labor delivery from 30 hrs to 20 hrs assuming a standard deviation of 10 These assumptions were based on a survey taken from the Labor and Delivery triage database for the 6 months prior to the study
The objective of this study was to investigate the effect of the use of both sonographic cervical length and fetal fibronectin on the length of outpatient triage and preterm labor interventions in symptomatic women with intact membranes
Methods
Study design This is a randomized trial of the use of transvaginal ultrasound cervical length and fetal fibronectin in women being evaluated for suspected PTL on labor and delivery at the Thomas Jefferson University Hospital Philadelphia between November 2004 and April 2006 The study was approved by the Internal Review Board
Gestational age was assigned by last menstrual period and first or early second trimester ultrasound If the last menstrual period was unknown or there was a discrepancy regarding the dates the ultrasound dating was used Eligible women who agreed to participate in the study were randomized to either a standard or a protocol arm At the time this study was initiated neither FFN nor CL were routinely used in the management of symptomatic women presenting to LD to be evaluated for PTL Women in the standard arm were evaluated without the results of the CL and FFN while women in the protocol arm were evaluated using the of the CL and FFN and managing physicians were asked to follow a specific PTL algorithm to determine a womens eligibility for treatment Physicians were encouraged to manage protocol patients according to the study recommended protocol for the use of FFN and CL which was reviewed with them for each patient on labor and delivery by a study investigator Once eligible for treatment the management of PTL was then left to the discretion of the physician
Definitions and study procedures
Before randomization all patients being evaluated for preterm labor were monitored in the triage area and uterine activity and fetal heart rate evaluated A speculum exam was performed to rule out ruptured membranes and to obtain a specimen for fetal fibronectin Specimens for fetal fibronectin were obtained with a Dacron swab from the posterior vaginal fornix and placed in buffer which then held on labor and delivery until the patient was either randomized determined to be ineligible or declined to participate in the study After randomization the specimen was immediately analyzed in our in house laboratory Samples were delivered to the laboratory within 1 hour of obtaining the sample and results were available within 1 hour Samples containing 50 ng or more per milliliter were designated as positive The FFN was delayed for 24-36 hours as needed if the patient had intercourse a pelvic exam or a transvaginal ultrasound within 24 hours A digital exam was then performed to determine dilatation and effacement of the cervix
Results of the fibronectin analysis were labeled by one of the study investigators after randomization so that only results from non-blinded specimens would be available to the managing physicians
Randomization was performed by means of computer generated random blocks of numbered sealed opaque envelops which were stratified in two groups based on gestational age 28 weeks and 28 weeks Each envelope was opened sequentially within each strata by one of the study investigators
Following randomization transvaginal ultrasound assessment of the cervix was performed Measurements were obtained using a 5-75 Mhz transvaginal probe placed in the anterior fornix after emptying the bladder The transducer was oriented to obtain a sagittal view of the cervix with the long axis view of the echogenic endocervical mucosa along the length of the canal The probe was withdrawn slightly until the image was blurred and enough pressure then reapplied to restore the image CL was measured from the internal to the external os along the endocervical canal At least three measurements were recorded over 5 minutes and the shortest best measurement in millimeters was used for the study
Using a two-sided t-test with alpha of 005 we calculated that a sample size of 45 patients in each group would have an 80 power to detect a 1 hour 33 in the mean time on labor delivery from 30 hrs to 20 hrs assuming a standard deviation of 10 These assumptions were based on a survey taken from the Labor and Delivery triage database for the 6 months prior to the study
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None