Trials / Completed
CompletedNCT04653792
Role Of Pregabalin To Decrease Postoperative Pain In Microdiscectomy
Role Of Pregabalin To Decrease Postoperative Pain In Microdiscectomy: A Randomized Clinical Trial
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 84 (actual)
- Sponsor
- Ziauddin University · Academic / Other
- Sex
- All
- Age
- 20 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare the effect of pregabalin in reducing the neuropathic pain in postoperative patients who have undergone single level Microdiscectomy for prolapsed intervetebral lumbar disc.
Detailed description
All patients were informed in detailed regarding the risk and complications and given written and informed consent, coming to our clinics were assessed by one of the senior team members of the spine, patient fulfilling the eligibility criteria were selected and included in the study. One week before the surgery the patients who met the eligibility criteria were randomized in a double-blind manner (participant and investigator) in a ratio of 1:1 into Group-A (Pregabalin 7mg, twice daily) or Group-B (Placebo, twice daily). The pain scores were recorded by VAS and Roland Morris score system on preoperative day compared to the scores on the 1st week postoperative follow-up.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Pregabalin 75mg | 75 mg capsule |
| DEVICE | Placebo | 75 mg |
Timeline
- Start date
- 2018-06-04
- Primary completion
- 2020-04-17
- Completion
- 2020-04-17
- First posted
- 2020-12-04
- Last updated
- 2020-12-04
Locations
1 site across 1 country: Pakistan
Regulatory
- FDA-regulated drug study
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT04653792. Inclusion in this directory is not an endorsement.