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Comparison of the effect of remifentanil and dexmedetomidine on surgeon satisfaction from surgical field and bleeding in rhinoplasty

Comparison of the effect of remifentanil and dexmedetomidine on surgeon satisfaction from surgical field and bleeding in rhinoplasty

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20141009019470N112
Enrollment
60
Registered
2021-04-01
Start date
2021-04-23
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

Rhinoplasty surgery. Encounter for cosmetic surgery

Interventions

Intervention 1: Intervention group: In the Intervention group one patients will receive 1 µg / kg dexmedetomidine (PFIZER, USA) for 20 minutes and at the same time as induction begins with a dose of 0

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 18-45 years old Patients undergoing rhinoplasty surgery time of surgery is 7-10 days before menstruation time

Exclusion criteria

Exclusion criteria: Patients with liver dysfunction Renal dysfunction Any known allergy or hypersensitivity to study drugs Abuse of analgesics and any addiction to opioid, Diabetes mellitus Hemorrhagic disease Using anticoagulants Cerebrovascular disease Heart block Cardiovascular disease Morbid obesity Females whom experience nausea and vomiting in their menstrual cycle Revision rhinoplasty surgery

Design outcomes

Secondary

MeasureTime frame
Patients’ satisfactions. Timepoint: After injection of intervention drugs in the recovery room and surgery ward. Method of measurement: Likert Scale.;Surgeon’ satisfactions. Timepoint: At the end of the surgery. Method of measurement: Likert Scale.

Primary

MeasureTime frame
Amount of intraoperative bleeding. Timepoint: At the end of the surgery. Method of measurement: Observasion.;Post operative pain. Timepoint: At arrival to the recovery room and at, 45,30,15 minutes. Method of measurement: Visual analogue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Nemati

Shiraz University of Medical Sciences

Nemati.mrym@gmail.com+98 71 3647 4270

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 13, 2026