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Analgesic efficacy of Paracervical Block versus Conscious Sedation in the manual vacuum aspiration of first trimester abortions; A randomized controlled trial

Analgesic efficacy of Paracervical Block versus Conscious Sedation in the manual vacuum aspiration of first trimester abortions; A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202504841468789
Enrollment
128
Registered
2025-04-15
Start date
2025-05-01
Completion date
Unknown
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy and Childbirth Abortions Anaesthesia

Interventions

Conscious sedation

Sponsors

IGE TOLUWALASE EBENEZER
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Women within the reproductive age group – 15 to 45 years, with first trimester abortion – at estimated gestational age of less than or equal to 13 weeks 2. Patients who are capable making informed decision and give written consent 3. Patients whose hemodynamic stability has been confirmed

Exclusion criteria

Exclusion criteria: 1. Hypovolemic shock 2. Septic abortion 3. Septic shock 4. Huge pelvic masses 5. Signs of peritonitis 6. Previous MVA attempts in index pregnancy 7. Neurological/ Psychiatric illness 8. History of adverse reaction to lidocaine, pentazocine or diazepam 9. Previous participation in the study 10. Neurogenic shock 11. Refusal of consent

Design outcomes

Primary

MeasureTime frame
The primary outcome of this study is the mean intraoperative pain score from both groups.

Secondary

MeasureTime frame
1. Comparing pain level prior to, and during the procedure in both groups 2. The need for additional analgesics in both groups 3. The side effect profile of medications used in both groups 4. Patient’s overall satisfaction in both groups

Countries

Nigeria

Contacts

Public ContactOLADELE ISOLA

SENIOR REGISTRAR

isolaoladele@gmail.com+2348139491238

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Feb 4, 2026