Skip to content

Prospective randomised double blind comparative study of cinnarizine versus placebo as prophylactic anti-travel sickness therapy in patients undergoing dy-case gynaecological surgery. - Cinnarizine Study

Prospective randomised double blind comparative study of cinnarizine versus placebo as prophylactic anti-travel sickness therapy in patients undergoing dy-case gynaecological surgery. - Cinnarizine Study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2004-002180-24-GB
Enrollment
272
Registered
2005-03-16
Start date
2005-04-12
Completion date
Unknown
Last updated
2019-12-10

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

Conditions

Post operative nausea and vomiting and motion sickness

Interventions

Trade Name: STUGERON Product Name: Cinnarizine Pharmaceutical Form: Tablet INN or Proposed INN: Cinnarizine CAS Number: CAS-298-57-7 Concentration unit: mg milligram(s) Concentration type: equal Conce

Sponsors

Swindon & Marlborough NHS Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Female patients 2. Undergoing day case gynaecological surgery 3. Aged 18-60 years 4. ASA 1 & 2 Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: 1. Those who are unable to give informed consent. 2. Patients with gastrointestinal disease. 3. Patients with hepatic or renal disease. 4. Pregnant or lactating patients. 5. Those patients with known or suspected adverse reactions to the study drugs. 6. Patients undergoing therapeutic termination of pregnancy. 7. Patients undergoing surgery for miscarriage. 8. Obese patients (BMI>30) 9. Patients suffering from pre-operative nausea or vomiting 10. Patients receiving current oral or intramuscular steroid therapy. 11. Patients suffering severe acute anxiety reactions. 12. Patients receiving other anti-emetic drugs

Design outcomes

Primary

MeasureTime frame
Main Objective: To investigate the clinical efficacy of a single post-operative dose of cinnarizine in the prevention of post-operative nausea and vomiting associated with the journey home after day-case gynaecological surgery.;Secondary Objective: ;Primary end point(s): Nausea, Retching and Vomiting.

Countries

United Kingdom

Outcome results

None listed

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