IRCT20160527028109N4RecruitingPhase 3
The effect of diluted ropivacaine in uterine distending fluid on pain after hysteroscopy surgeries
Trial Snapshot
- Phase
- Phase 3
- Status
- Recruiting
- Enrollment
- 60
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 years to 40 years (—)
- Sex
- Female
Inclusion Criteria
- •Women candidates for hysteroscopy treatment based on the opinion of a specialist
- •Conscious consent to participate in the study
Exclusion Criteria
- •Existence of pelvic inflammatory disease
- •Having known cervical malignancy, severe uterine bleeding, cervical conization
- •Need for intraoperative surgery due to complications (such as laparotomy due to uterine perforation)
- •Having psychological or neurological disorders that affect pain perception.
- •Allergy to rupivacaine
- •Reluctance to continue cooperation while studying
- •Patients with chronic diseases with pain such as low back pain, etc. who use continuous painkillers.
- •Patients have previously had a tubectomy or have a bilateral obstruction of the tube.
- •Patients with preoperative pelvic pain, dyspareunia, dysmenorrhea, with a vas score of 3 or higher.
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