Trials / Completed
CompletedNCT02714231
Oral Diclofenac Sodium Versus Oral Hyoscine Butyl Bromide During Intrauterine Device Insertion
A Randomized Controlled Trial of 2 Different Methods for Pain Relief During Intrauterine Device Insertion
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 100 (actual)
- Sponsor
- Assiut University · Academic / Other
- Sex
- Female
- Age
- 20 Years – 50 Years
- Healthy volunteers
- Not accepted
Summary
The aim of our study is to compare the analgesic effect of oral diclofenac sodium versus oral hyoscine butyl bromide during intrauterine device insertion.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | diclofenac sodium (cataflam) | The patients in the study group will take one tablet of cataflam 50 mg 30 min before the scheduled time of the procedure |
| DRUG | hyoscine butyl bromide (buscopan) | The patients in the study group will take one tablet of buscopan 10 mg 30 min before the scheduled time of the procedure |
Timeline
- Start date
- 2016-03-01
- Primary completion
- 2017-02-01
- Completion
- 2017-03-01
- First posted
- 2016-03-21
- Last updated
- 2017-07-19
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT02714231. Inclusion in this directory is not an endorsement.