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Ketoprofen With or Without Vaginal Isonicotinic Acid Hydrazide Prior to Hysterosalpingography

A

Aswan University Hospital

Status

Completed

Conditions

Infertility, Female

Treatments

Drug: Ketoprofen + placebo
Drug: Ketoprofen + INH

Study type

Interventional

Funder types

Other

Identifiers

NCT04500470
aswu/351/3/19

Details and patient eligibility

About

The aim of our study is to determine the efficacy of Ketoprofen with or without vaginal isonicotinic acid hydrazide on the pain scores during HSG.

Full 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

Enrollment

200 patients

Sex

Female

Ages

18 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • any patient came for Hysterosalpingography

Exclusion criteria

  • any patient has contraindication to HSG

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

200 participants in 2 patient groups, including a placebo group

Group A
Experimental group
Description:
patients will have of oral Ketoprofen 60 minutes before the procedure plus 3 table 900 mg vaginal isonicotinic acid hydrazide by the patient 12 hours before the procedure
Treatment:
Drug: Ketoprofen + INH
Group B
Placebo Comparator group
Description:
patients will have of oral Ketoprofen 60 minutes before the procedure plus 3 table vaginal placebo by the patient 12 hours before the procedure
Treatment:
Drug: Ketoprofen + placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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