Skip to content

Effect of Granisetron in prevention of shivering after spinal anesthesia in lower Abdominal Surgery

Effect of Granisetron in prevention of shivering after spinal anesthesia in lower Abdominal Surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201411203915N14
Enrollment
105
Registered
2014-12-09
Start date
2014-03-21
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

Shivering after regional anesthesia. Complications of medical and surgical care

Interventions

Intervention 1: Group A : Administration of intavenous granisetrone 1mg before spinal anesthesia. Intervention 2: Group B: Administration of intravenous granisetrone 3 mg befor spinal anesthesia. Inte
Treatment - Drugs
Group A : Administration of intavenous granisetrone 1mg before spinal anesthesia
Group B: Administration of intravenous granisetrone 3 mg befor spinal anesthesia
group C: Administration of intravenous saline normal 5 ml before spinal anesthesia

Sponsors

Research Vice Chancellor for Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: ages 18-60 yr; American society of anesthesia (ASA) class 1-2; elective inguinal hernia repair with spinal anesthesia. Exclusion criteria: patients refuse of spinal anesthesia; any contraindication for regional anesthesia.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Post-operative shivering. Timepoint: Till 2 hours after surgery. Method of measurement: Clinical assessment.

Secondary

MeasureTime frame
Need for petidine administration. Timepoint: Till 2 hours after surgery. Method of measurement: Clinical assessment.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Ali Peirovifar

Tabriz University of Medical Sciences

peirovifara@gmail.com+98 41 3334 7054

Outcome results

None listed

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