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The effect of intravenous administration of Dexmedethomidine on the duration of ultrasound-guided supraclavicular brachial plexus block in comparison with Propofol, in patients undergoing upper extremity surgery in Shariati hospital

The effect of intravenous administration of Dexmedethomidine on the duration of ultrasound-guided supraclavicular brachial plexus block in comparison with Propofol, in patients undergoing upper extremity surgery in Shariati hospital

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017051734005N1
Enrollment
88
Registered
2017-07-17
Start date
2017-06-22
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

Local anaesthetics. Local anaesthetics

Interventions

Treatment - Drugs
Intervention 1: groupB: supraclavicular injection of 25 ml of bupivacaine 0.5% and of propofol 50 mcg / kg / min intravenously. Intervention 2: groupA: supraclavicular injection of 25 ml of bupivacai
groupB: supraclavicular injection of 25 ml of bupivacaine 0.5% and of propofol 50 mcg / kg / min intravenously.
groupA: supraclavicular injection of 25 ml of bupivacaine and 0.5 mg / kg / min of dexamethmonide intravenously

Sponsors

Tehran University Of Medical Sciences Vice Chancellor Of Research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age between 20-50 years old; ASA class III, II, I; BMI less than 35; no history of drug allergy; satisfaction of the patient and filling out the consent form. Exclusion criteria: failure to perform supraclavicular block; duration of surgery for more than 180 minutes; cancellation of operation; occurrence of surgical complication during surgery; the need for general anesthesia.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sensory block onset. Timepoint: sensory block will be checked continuously after completion of injection until complete sensory and motor block. Method of measurement: pinprick test and a verbal rating scale from 100% (normal sensation) to 0 (no sensation).;Sensory block duration. Timepoint: after complete sensory block and every 15 minutes following the end of operation. Method of measurement: pinprick test and a verbal rating scale from 100% (normal sensation) to 0 (no sensation).;Motor block onset. Timepoint: motor block will be checked continuously after completion of injection until complete motor block. Method of measurement: Lovett rating scale.;Motor block duration. Timepoint: after complete motor block and every 15 minutes following the end of operation. Method of measurement: the Lovett rating scale.

Secondary

MeasureTime frame
Systolic blood pressure. Timepoint: continuously monitoring while the surgery is performing. Method of measurement: manometer.;Diastolic blood pressure. Timepoint: continuously monitoring while the surgery is performing. Method of measurement: manometer.;Heart rate. Timepoint: continuously monitoring while the surgery is performing. Method of measurement: Monitoring.;Respiratory depression. Timepoint: continuously monitoring while the surgery is performing. Method of measurement: O2 saturation & Respiratory Rate.;Drug consumption in the 24 hours after surgery. Timepoint: patient need. Method of measurement: Medical records.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Fatemeh Elmi

Shariati Hospital, Anesthesilogy Department

f-elmi@student.tums.ac.ir+98 21 2221 9958

Outcome results

None listed

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