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Completed

NCT Number: NCT02714231

Oral Diclofenac Sodium Versus Oral Hyoscine Butyl Bromide During Intrauterine Device Insertion

The aim of our study is to compare the analgesic effect of oral diclofenac sodium versus oral hyoscine butyl bromide during intrauterine device insertion.

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Key information

Conditions

Family Planning

Age range

20 year–50 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 4

Primary location

Ahmed Abbas

Assiut, Cairo Governorate, 002, Egypt

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women not taken analgesics or anxiolytics in the 24 hours prior insertion
  • Women not taken misoprostol prior to intrauterine device insertion
  • Women who will accept to participate in the study

Exclusion criteria

  • Any contraindication to intrauterine device placement

Treatment and study plan

diclofenac sodium (cataflam)

Drug

The patients in the study group will take one tablet of cataflam 50 mg 30 min before the scheduled time of the procedure

hyoscine butyl bromide (buscopan)

Drug

The patients in the study group will take one tablet of buscopan 10 mg 30 min before the scheduled time of the procedure

Primary outcomes

  1. Mean pain score during insertion

    Time frame: intraoperative

Secondary outcomes

  1. Patient satisfaction score

    Time frame: 5 minutes

Sponsors and collaborators

Lead sponsor

Assiut University

Other

Registry information

Official study title

A Randomized Controlled Trial of 2 Different Methods for Pain Relief During Intrauterine Device Insertion

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Mar 21, 2016
Registry last updated
Jul 19, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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