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Buscopan for pain control in manual vacuum aspiration (MVA): A randomized controlled trial

Buscopan for pain control in manual vacuum aspiration (MVA): A randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800014590
Enrollment
Unknown
Registered
2018-01-23
Start date
2018-01-30
Completion date
Unknown
Last updated
2023-04-12

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

Conditions

miscarriage

Interventions

Two groups:Buscopan intravenous injection, 1ml 20mg once versus normal saline intravenous injection 1 ml once

Sponsors

Prince of Wales Hospital, The Chinese University of Hong Kong
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Women 18 years old or above; 2. first trimester miscarriage; 3. No fetal heart beat in those with CRL 25mm; 4. incomplete miscarriage with POG <5cm; 5. hemodynamically stable; 6. tolerates well with speculum examination.

Exclusion criteria

Exclusion criteria: 1. cervical stenosis; 2. fibroid uterus >12 weeks in size; 3. known uterine malformation; 4. bleeding disorder; 5. clinically sepsis; 6. inability to tolerate pelvic examination; 7. History of allergy to misprostol, Buscopan? or same group of drug; 8. Contraindication to the use of Buscopan?; 9. Unable to follow instruction to have saliva sampling; 10. History of psychological/ psychiatric problem; 11. History of smoking, physical exercise, meals, alcoholic beverages and low pH drinks at least 1 hour prior to saliva sampling.

Design outcomes

Primary

MeasureTime frame
To investigate the use of Buscopan in reducing pain level during MVA procedure;

Secondary

MeasureTime frame
To investigate the use of Buscopan in reducing stress level during MVA procedure;

Countries

China

Contacts

Public ContactDr. CHUNG Pui Wah, Jacqueline

Department of OG, CUHK

jacquelinechung@cuhk.edu.hk+852 35051537

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026