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Title: Effect of Clonidine on Post-operative Nausea and Vomiting in Breast Cancer Surgery

Title: Effect of Clonidine on Post-operative Nausea and Vomiting in Breast Cancer Surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20141009019470N99
Enrollment
68
Registered
2020-06-18
Start date
2020-07-21
Completion date
Unknown
Last updated
2020-07-13

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

Conditions

Breast Cancer. Intraductal carcinoma in situ of unspecified breast

Interventions

Intervention 1: Intervention group:Patients are given 0.2 mg of clonidine tablets in the morning. Intervention 2: Control group:Control group: Patients are given one tablet in the morning as a placebo

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients Candidate for Breast Cancer Surgery Ages 15 to 70 years ASA Class I-II General Anesthesia

Exclusion criteria

Exclusion criteria: A history of postoperative nausea and vomiting Patients who have received antiemetic drugs such as ondansetron or dexamethasone 24 hours before surgery History of motion sickness Allergy to Propofol and Clonidine Concomitant use of beta-blocker medication that may affect a patient's heart rate Systolic blood pressure less than 100 History of using Steroid History of myocardial infarction History of tricyclic antidepressant use History of kidney dysfunction

Design outcomes

Primary

MeasureTime frame
Post-operative Nausea and Vomiting. Timepoint: Postoperative nausea and vomiting in recovery is recorded at 0-15-30 and 45 minutes. After transferring the patient to the surgical ward, the incidence of postoperative nausea and vomiting is evaluated at 6 and 24 hours. Method of measurement: Likert.

Secondary

MeasureTime frame
Hemodynamic changes. Timepoint: Blood pressure and heart rate are recorded in the surgical ward in the operating room before induction after induction and in recovery at 0-15-30 and 45 minutes.After transferring the patient to the surgical ward, the patient's blood pressure is checked at 24,2,4,6,12 hours. Method of measurement: Monitoring.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShabnam Heidarynezhad

Shiraz University of Medical Sciences

shab.hn1998@gmail.com+98 71 3674 4270

Outcome results

None listed

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