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Effect of of dexmedetomidine in control bleeding during sinus surgery

Effect of intravenous infusion of dexmedetomidine in control bleeding during functional endoscopic sinus surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017012929256N2
Enrollment
60
Registered
2017-03-04
Start date
2016-04-03
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

Haemorrhagic condition. Haemorrhagic condition, unspecified

Interventions

Intervention 1: Intervention group: After induction of anesthesia 1µ/ kg/min Dexmedtomidin be injected within 10 minutes, then dexmedtomidin infusion begins with 0.5 µ /kg/minute. Intervention 2: Con
Treatment - Drugs
Intervention group: After induction of anesthesia 1µ/ kg/min Dexmedtomidin be injected within 10 minutes, then dexmedtomidin infusion begins with 0.5 µ /kg/minute.
Control group: After induction of anesthesia, 50 ml normal saline as placebo administrated.

Sponsors

Vice-Chancellor for Research and Technology of Ahvaz Jundishapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients undergoing endoscopic sinus surgery; aged between 16 and 60 years; ASA class I and II. Exclusion Criteria: diabetes mellitus; coagulation disorders; kidney and liver dysfunction; cerebrovascular disease; cardiovascular disease; high blood pressure; asthma; chronic obstructive pulmonary disease; psychiatric patients; drug allergy; taking beta-blockers; heart rate of less than 55.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Bleeding. Timepoint: q 15 minute up to the end of anesthesia. Method of measurement: data collected from standard operting room monitoring systems.

Secondary

MeasureTime frame
Nausea and vomit. Timepoint: every 30 minutes during 2 hours recovery time. Method of measurement: VAS score.;Awakening time. Timepoint: after injection of neuromascular blockade. Method of measurement: time after reversal of neuromasculare blockade till eye opening on command.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSharzad Pooyan

Ahvaz Jundishapor University of Medical Sciences

sheripooya@yahoo.com+98 61 3571 5794

Outcome results

None listed

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