Ignite Creation Date:
2024-05-06 @ 4:06 PM
Last Modification Date:
2024-10-26 @ 2:04 PM
Study NCT ID:
NCT04874675
Status:
SUSPENDED
Last Update Posted:
2023-01-05
First Post:
2021-04-28
Brief Title:
An Randomized Control Trial Comparing Two Drug Combinations for Pain Management After Third Molars Surgery
Sponsor:
University of Zimbabwe
Organization:
University of Zimbabwe
Study Overview
Official Title:
A Randomised Control Clinical Trial Comparing Diclofenac Acetaminophen Codeine and IbuprofenAcetaminophenCodeine Combination for Pain Management After Third Molars Surgery
Status:
SUSPENDED
Status Verified Date:
2023-01
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Covid 19 lockdown
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Randomised control clinical trial to compare which combination of analgesics in effective in pain management after third molar extraction of wisdom teeth The study will assess post operative pain after third molar extraction of two groups of study participants who will be given one of the two combinations of Diclofenac acetaminophencodeine and ibuprofenacetaminophencodeine
Detailed Description:
Double blind randomized control clinical trial to compare the level of pain relief that occurs after third molar extraction done under local anaesthesia at the maxillofacial center Harare Zimbabwe The participants will be randomized into two arms upon fitting the inclusion criteriaThe pharmacist will be in charge of randomization and will randomise the participants upon giving them the medications One group will receive combination of diclofenacacetaminophencodeine and the other group will receive ibuprofenacetaminophencodeine as post extraction analgesiaThe dosages of the medications will be Diclofenac 50mg ibuprofen 400mg acetaminophen 500mg and codeine 15mg respectively Questionnaires will be given to the patient to complete after discharge from the surgery and other parts of the questionnaire will be completed on review after 7 days A record will be done of the postoperative pain experience using visual analogue scale use of rescue medication and details pertaining to impacted tooth
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?:
None