Skip to content

Pain control in the surgical management of incomplete miscarriages at Princess Marina Hospital; a randomized controlled trial comparing paracervical block, conscious sedation, and a combination of both methods

Pain control in the surgical management of incomplete miscarriages at Princess Marina Hospital; a randomized controlled trial comparing paracervical block, conscious sedation, and a combination of both methods

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
PACTR
Registry ID
PACTR202502619751607
Enrollment
210
Registered
2025-02-03
Start date
2025-03-01
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Pain control during surgical management of first trimester incomplete miscarriages

Interventions

paracervical block which is Group A
Paracervical block with conscious sedation which is Group C
Conscious Sedation

Sponsors

Catherine Raletsatsi
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: • Women with the diagnosis of incomplete miscarriage at a gestational age of ?13weeks of gestation who have any of the following; 1.Vaginal examination showing cervical Os dilatation of 1cm or more with the product of conception extruding from the cervical Os and patient is actively bleeding 2.Bedside ultrasound confirming retained product of conception and patient is actively bleeding 3.Any patient with an open cervical os and evidence of retained products who is not actively bleeding and opts for surgical management after counselling

Exclusion criteria

Exclusion criteria: 1.Patients who cannot consent on their own without need of a guardian 2. Patients with a known history of an allergy to the drugs 3. Hemodynamically unstable patients meeting a diagnosis of either septic or hypovolemic shock 4.Patients with non-anaesthesia related complications of abortion

Design outcomes

Primary

MeasureTime frame
• Pain control across the 3 methods of analgesia being studied • Complications of the 3 methods of analgesia being studied

Secondary

MeasureTime frame
1.Recovery time post procedure 2.Overall patient satisfaction

Countries

Botswana

Contacts

Public ContactSarah Hanson

University of Botswana Lecture

hansonsj@gmail.com+26777907521

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026