Clinical Trials Directory

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

TypeNameDescription
DRUGcelecoxib plus lidocaineCelecoxib 200 mg (Celebrex® 200, Pfizer,USA) administered orally 2 h before the procedure +10% lidocaine spray 4 puffs during the procedure
DRUGCelecoxibCelecoxib 200 mg (Celebrex® 200, Pfizer,USA) administered orally 2 h before the procedure +Sterile water 4 puffs during the procedure
DRUGlidocaineplacebo 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.