Compression of addition of Dexmedetomidine and fentanyl to Lidocain management pain in curettage proceeded

Phase 2

Recruiting

• Conditions: curettage.; Pregnancy with abortive outcome; O00-O08

• Registration Number: IRCT20141209020258N162
• Lead Sponsor: Arak University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 30 August 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 132

Inclusion Criteria

18 to 40 years old
Candidate for curettage up to 14 weeks of pregnancy

Exclusion Criteria

Dissatisfaction

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Up to 2 hours after surgery. Method of measurement: Visual analog pain questionnaire.;Nausea and vomiting. Timepoint: After surgery. Method of measurement: Observation.;Mean of drugs consumed. Timepoint: After surgery. Method of measurement: Observation.