Ignite Creation Date:
2024-10-26 @ 3:36 PM
Last Modification Date:
2024-10-26 @ 3:36 PM
Study NCT ID:
NCT06532318
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-07-29
Brief Title:
Comparative Study Between Platelet Rich Plasma and Steroid Injection in Trigger Finger Treatment
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Comparative Study Between Intralesional Injection of Platelet Rich Plasma and Intralesional Steroid for the Treatment of Trigger Finger in Black Patients
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The goal of this clinical trial is to learn if platelet rich plasma works to treat early stage trigger finger in adults It will also learn about the safety platelet rich plasma The main questions it aims to answer are
Does platelet rich plasma lower the pain associated with trigger finger of participants Does it improve the hand grip strength and Q DASH score of participants Researchers will compare platelet rich plasma to Depo-Medrol steroid a known standard of care for early stage trigger finger to see if platelet rich plasma works to treat early trigger finger
Participants will
Take platelet rich plasma or a depo-medrol steroid intralesional injection at recruitment into the intervention Visit the clinic once every 4 weeks for checkups and parameter measurements Investigator will will keep a record of participants progress in symptom remission
Does platelet rich plasma lower the pain associated with trigger finger of participants Does it improve the hand grip strength and Q DASH score of participants Researchers will compare platelet rich plasma to Depo-Medrol steroid a known standard of care for early stage trigger finger to see if platelet rich plasma works to treat early trigger finger
Participants will
Take platelet rich plasma or a depo-medrol steroid intralesional injection at recruitment into the intervention Visit the clinic once every 4 weeks for checkups and parameter measurements Investigator will will keep a record of participants progress in symptom remission
Detailed Description:
None
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