Skip to content

The comparation effect of general anesthesia verses spinal on outcome of laminectomy

The effect of general anesthesia and spinal on laminectomy

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015062222870N1
Enrollment
50
Registered
2015-09-21
Start date
2015-07-23
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

laminectomy. vertebral column

Interventions

Intervention 1: Intervention group 2: In spinal group patients using bupivacaine 5% , 15 mg intrathecally at L3 - L4 or L4 - L5 space in the sitting position were included in the study . bupivaca
Treatment - Drugs
Intervention group 2: In spinal group patients using bupivacaine 5% , 15 mg intrathecally at L3 - L4 or L4 - L5 space in the sitting position were included in the study . bupivacaine manufact
Intervention group 1: In general anesthesia group using propofol (2-3 Mg/Kg), 50% O2, 50% N2o, fentanyl, isoflurane and atracurium patients was undergoing surgery. propofol,fentanyl and isoflurane

Sponsors

Vice chancellor for research, Ilam University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age 18-65 year; same surgeon and anesthesia. Exclusion criteria: lack of patient agreement for spinal anesthesia; systemic disease; reaction of spinal anesthesia drug.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Shivering. Timepoint: After intervention in recovery. Method of measurement: checklist and VAS.;Bleeding. Timepoint: During intervention in surgery time. Method of measurement: Pad.;Pain. Timepoint: After intervention during 1,4,8,12,24 h after surgery. Method of measurement: Visual Analogue Scale (VAS).;Nausea & Vomiting. Timepoint: After intervention in recovery. Method of measurement: Checklist.;Blood pressure. Timepoint: During intervenation under surgery. Method of measurement: sphygmomanometer.;Hart rate. Timepoint: During intervenation under surgery. Method of measurement: Pulse oximeter.

Secondary

MeasureTime frame
Cost. Timepoint: After intervention during discharge. Method of measurement: checklist.;Drug consumption. Timepoint: during 24 h after intervenation. Method of measurement: according to Mg.;Surgeon satisfaction. Timepoint: After intervention. Method of measurement: Questionnaire.;Patients satisfaction. Timepoint: After intervention. Method of measurement: Questionnaire.;The first movement time. Timepoint: After intervention. Method of measurement: according to time duration after surgery.;Length of hospital stay. Timepoint: After intervention. Method of measurement: according to time duration of stay.;Duration of recovery room. Timepoint: After intervention. Method of measurement: according to time duration.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Khani

Ilam University of Medical Sciences

nimakhani@gmail.com; khani-a@medilam.ac.ir+98 84 3333 7259

Outcome results

None listed

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