Trials / Completed
CompletedNCT04505657
Lidocaine Spray Plus Oral Celecoxib for Pain Control During Hysterosalpingography
Lidocaine Spray Plus Oral Celecoxib for Pain Control During Hysterosalpingography: a Randomized Controlled Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 150 (actual)
- Sponsor
- Aswan University Hospital · Academic / Other
- Sex
- Female
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Not accepted
Summary
our aims to investigate the effectiveness of10% Lidocaine Spray plus oral celecoxib for Pain Control During Hysterosalpingography
Detailed description
hysterosalpingography can cause pain and discomfort in several ways: Use of the tenaculum to grasp the cervix and straighten the uterus for proper insertion; trans-cervical actions including measuring uterine depth, inserting the cannula; and injection of the dye
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | celecoxib plus lidocaine | Celecoxib 200 mg (Celebrex® 200, Pfizer,USA) administered orally 2 h before the procedure +10% lidocaine spray 4 puffs during the procedure |
| DRUG | Celecoxib | Celecoxib 200 mg (Celebrex® 200, Pfizer,USA) administered orally 2 h before the procedure +Sterile water 4 puffs during the procedure |
| DRUG | lidocaine | placebo to celecoxib administered orally 2 h before the procedure +10% lidocaine spray 4 puffs during the procedure |
Timeline
- Start date
- 2020-09-01
- Primary completion
- 2021-06-30
- Completion
- 2021-09-27
- First posted
- 2020-08-10
- Last updated
- 2021-09-29
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT04505657. Inclusion in this directory is not an endorsement.