Skip to content

Comparison of efficacy of two methods of Intera venous regional anesthesia

Comparison of efficacy of two methods of Intera venous regional anesthesia: Use of one tourniquet versus traditional method in upper limb surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013041111898N4
Enrollment
80
Registered
2013-05-07
Start date
2013-05-22
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

Fracture of upper limb. Incl.: Broken arm NOS Fracture of arm NOS. The following subdivisions are provided for optional use in a supplementary character position where it is not possible or not desired to use multiple coding to identify fracture and open wound

Interventions

Intervention 1: Changing tourniquet and If remain pain narcotic is injected. Intervention 2: Injection narcotic.
Changing tourniquet and If remain pain narcotic is injected
Injection narcotic

Sponsors

Research and Technology Department, Guilan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients' age limit from 50 to 20 years, ASA class I, orthopedic surgery with orthopedic interest has been detected in less than 60 minutes. Exclusion criteria: Obesity, peripheral vascular disease, Raynaud's phenomenon, scleroderma, Epilepsy, sickle cell anemia, Methemoglobin, patients with any history of drug allergies and diseases such as heart disease - smoking, high blood pressure, coagulation disorders, excessive bleeding, Hb less than 10, use Calcium Canal Blockeror Beta blocker, renal failure, drug abuse and patient who did not have necessary cooperation and skin infection in axillary region

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
VAS Score. Timepoint: 0, 15, 30 & 60 min after complete sensory block occurs. Method of measurement: with VAS score based on patient report.;Complications. Timepoint: 0, 15, 30 & 60 min after complete sensory block occurs. Method of measurement: Based on clinical judgment, with agitation, anxiety, seizures, impaired consciousness, cardiovascular complications.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Sadeq Mousavi

Medical Student

arman.mousavi1989@gmail.com+98 13 1555 2241

Outcome results

None listed

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