Clinical Trials Directory

Trials / Completed

CompletedNCT06140238

Preemptive Analgesic Efficacy of Parecoxib for Reducing Postoperative Pain in Gynecological Surgery

Preemptive Analgesic Efficacy of Parecoxib for Reducing Postoperative Pain in Gynecological

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
178 (actual)
Sponsor
Department of Medical Services Ministry of Public Health of Thailand · Other Government
Sex
Female
Age
18 Years – 70 Years
Healthy volunteers
Accepted

Summary

The research is to test the preemptive analgesic efficacy of Parecoxib drug in gynecological surgery by comparing Parecoxib drug and NSS administration 15 min before starting the surgery which the result of postoperative pain score is interpret by visual analog scale index

Detailed description

The research is working on testing the preemptive analgesic efficacy of Parecoxib drug in gynecological surgery whether its can reduce postoperative pain score, reduce total opioid consumption in first 24 hour postoperation and reduce postoperation hospital length stay. Patients who are undergoing gynecological surgery is recruited to the research project while they admit in the hospital for preoperative preparation, in each type of surgery groups (1.Total abdominal hysterectomy 2. Adnexal surgery 3. Surgical staging) will divided in to 2 groups which is experimental group (Parecoxib) and control group (Normal saline). The experimental group will have Parecoxib administration 15 min before starting the surgery and control group will have normal saline administration 15 min before starting the surgery as same, the primary result is postoperative pain score which is interpreted by Visual analog scale index at 2,6,12,24 hour postoperation, the patients will get opioid drug (Morphine) for pain control depending on pain score index they inform, if pain score \>7: morphine 0.075 mg/kg iv, if pain score 5 : morphine 0.05mg/kg iv, if pain score \<5 : no morphine given. Lastly the side effect of Parecoxib drug will be observed and postoperative hospital length stay of each patient will be recorded

Conditions

Interventions

TypeNameDescription
DRUGParecoxibParecoxib administration 15 minutes before start surgical operation
DRUGNormal salineNormal saline administration 15 minutes before start surgical operation

Timeline

Start date
2023-09-10
Primary completion
2024-04-27
Completion
2024-06-27
First posted
2023-11-18
Last updated
2024-11-14

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT06140238. Inclusion in this directory is not an endorsement.