Management of pain due to Intra Uterine Copper Device (Copper T) insertion with Drotaverine and Mefenamic acid
Not Applicable
Completed
- Registration Number
- CTRI/2014/05/004580
- Lead Sponsor
- All India Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 36
Inclusion Criteria
healthy females Seeking intrauterine device as contraception
Exclusion Criteria
(1) Pregnancy;
(2) Having a known sensitivity to nonsteroidal anti-inflammatory drugs, lignocaine; (3) Having peptic ulcer disease, inflammatory bowel disease, porphyrias, genital
infections, undiagnosed vaginal bleeding cervical stenosis, serious cardiac
disease;
(4) Being unable or unwilling to provide informed consent;
And
(5) Having history of cervical surgery.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method PAIN SCORES(VAS)Timepoint: 4 hours and 5 days
- Secondary Outcome Measures
Name Time Method Adverse effects of drugsTimepoint: 0,15 min,30 min