Evaluation of paracervical block versus conscious sedation for pain relief during manual vacuum aspiration: A randomized controlled trial
Not Applicable
Recruiting
- Conditions
- Anaesthesia
- Registration Number
- PACTR202404574700044
- Lead Sponsor
- Emmeh Sweiyi Fiddo
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 66
Inclusion Criteria
Women who give consent.
Women at less than 13 weeks gestation with incomplete abortion.
Exclusion Criteria
Women with psychiatric or neurological disorders.
Women with an allergy to Lignocaine, Pentazocine and/or Diazepam.
Women with septic abortion.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Mean pain scores of participants who will receive either form of analgesic agent. Need for additional analgesia intraoperatively.
- Secondary Outcome Measures
Name Time Method Incidence of side effects experienced with either analgesic agent. Participant satisfaction with assigned analgesic.