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Comparison of anesthesia by sodium thiopental with propofol in reducing the need for opiate after tibiofibular fracture surgery

Comparison of anesthesia by sodium thiopental with propofol in reducing the need for opiate after tibiofibular fracture surgery

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017110733202N6
Enrollment
173
Registered
2017-11-12
Start date
2017-10-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Reducing the need for opiate after tibiofibular fracture surgery. Fracture of bone following insertion of orthopaedic implant, joint prosthesis, or bone plate Excl.: complication of internal orthopaedic devices, implants or grafts (T84.-)

Interventions

Intervention 1: Intervention group: After placement of patients on the bed, the necessary monitoring is performed and all injections of midazolam (0.05 mg / kg) and morphine (0.1 mg / kg) are given as
Treatment - Drugs
Intervention group: After placement of patients on the bed, the necessary monitoring is performed and all injections of midazolam (0.05 mg / kg) and morphine (0.1 mg / kg) are given as premedication.
Control group: After placement of patients on the bed, the necessary monitoring is performed and all injections of midazolam (0.05 mg / kg) and morphine (0.1 mg / kg) are given as premedication. 0.5

Sponsors

Vice Chancellor for research of Sabzevar University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
15 Years to 45 Years

Inclusion criteria

Inclusion criteria: exclusion criteria: In case of anxiety and lack of response to fentanyl; Surgery longer than 2 hours; All people with a history of systemic disease (cardiovascular, respiratory, hypertension, diabetes, etc.); Patients at risk for nausea and vomiting; Patients with drug addiction or drug addiction. Inclusion criteria: Have personal consent; Surgery is elective.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: 1-2-3-4 hours after surgery. Method of measurement: Visual Scale of Pain.;Heart rate. Timepoint: 1-2-3-4 hours after surgery. Method of measurement: Examination.;Narcotic. Timepoint: 1-2-3-4 hours after surgery. Method of measurement: MG.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Nematshahi

Sabzevar University of Medical Sciences

9151737407mn@gmail.com+98 51 4401 1028

Outcome results

None listed

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