Trials / Completed
CompletedNCT03652116
Bupivacaine Verus Pethidine for Post Cesarean Section Pain Relief
Subrectal and Subcutaneous Wound Infiltration With Bupivacaine Versus Pethidine for Postcesarean Section Pain Relief: a Randomized Clinical Trial
- Status
- Completed
- Phase
- Phase 2 / Phase 3
- Study type
- Interventional
- Enrollment
- 78 (actual)
- Sponsor
- Ain Shams University · Academic / Other
- Sex
- Female
- Age
- 18 Years – 40 Years
- Healthy volunteers
- Not accepted
Summary
The aim of this study is to compare between the effect of wound infiltration with bupivacaine or pethidine for post cesarean section pain relief.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Wound infiltration by Bupivacaine | Subcutaneous and subrectal infiltration with 0.25 % Bupivacaine diluted in 20 ml normal saline before closure of the wound |
| DRUG | Wound infiltration by Pethidine | Subcutaneous and subrectal infiltration with 50 mg pethidine diluted in 20 ml normal saline before closure of the wound |
Timeline
- Start date
- 2017-04-21
- Primary completion
- 2018-06-10
- Completion
- 2018-08-01
- First posted
- 2018-08-29
- Last updated
- 2018-08-31
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT03652116. Inclusion in this directory is not an endorsement.