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Comparison of block quality and complications after spinal anesthesia using two different doses marcaine and fentanyl in leg fracture surgery in opium abusers

Comparison of block quality and complications after spinal anesthesia using two different doses marcaine and fentanyl in leg fracture surgery in opium abusers

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
IRCT
Registry ID
IRCT20210218050400N2
Enrollment
80
Registered
2021-03-16
Start date
2021-02-27
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

Fracture. Fracture of lower limb, level unspecified

Interventions

Intervention 1: Control group:All patients undergo spinal anesthesia after receiving 10 cc / kg of intravenous crystalloid solution by the executor in a sitting position on the vertebral surfaces (L5-

Sponsors

Birjand University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients who are candidates for leg fracture surgery (non-emergency) referred to Imam Reza (AS) Hospital in Birjand

Exclusion criteria

Exclusion criteria: Patients with coagulation problems Addiction Emergency surgery Duration of surgery lasting more than two hours Change in anesthesia during surgery Uncontrolled comorbid disease (ASA3 and above) History of postoperative bleeding Coagulation heart disease or infectious Known allergy to amide anesthetics Use of psychotropic drugs

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 1-2-3-4-8-12 hours after the measurement operation. Method of measurement: VAS.;Nausea. Timepoint: 1-2-3-4-8-12 hours after the measurement operation. Method of measurement: The patient is asked if he or she feels overwhelmed or upset.;Vomiting. Timepoint: 1-2-3-4-8-12 hours after the measurement operation. Method of measurement: The patient is asked.;Itching. Timepoint: 1-2-3-4-8-12 hours after the measurement operation. Method of measurement: The patient is asked.;Need for pain killers. Timepoint: 1-2-3-4-8-12 hours after the measurement operation. Method of measurement: Based on the onset of pain and the patient's first request for analgesia.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSomayeh Sabaghiyan Delosi

Birjand University of Medical Sciences

habibe.momeni@gmail.com+98 56 3290 4004

Outcome results

None listed

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