Clinical Trials Logo
  1. Home
  2. Anesthetics
  3. NCT01140100
  4. Details
NCT01140100 Clinical Trial

A Comparative Study of Depth of Anesthesia Monitored by Bispectral Index (BIS) Values

Anesthetics Clinical Trial

Official title:
A Comparative Study of Depth of Anesthesia Monitored by BIS Values in Two Anesthesia Techniques

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01140100
Other study ID # 85-3211
Secondary ID
Status Completed
Phase Phase 2
First received June 8, 2010
Last updated June 8, 2010

Study information
Verified date January 2007
Source Shiraz University of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority Iran: Ministry of Health
Study type Interventional

Clinical Trial Summary

The aim of this study is to determine whether induction of anesthesia with thiopental followed by propofol infusion is able to maintain sufficient depth of anesthesia .

Recruitment information / eligibility
Status Completed
Enrollment 82
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- being adult

- having ASA I or II

- scheduled for elective cataract surgery under general anesthesia

Exclusion Criteria:

- massive obesity

- intake of any central nervous system (CNS) stimulants

- intake of CNS depressants

- intake of Tricyclic antidepressants

- known adverse reaction to the study drugs

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• propofol

• thiopental,propofol

Locations
Country Name City State
Iran, Islamic Republic of Shiraz University of Medical Sciences Shiraz Fars

Sponsors (1)
Lead Sponsor Collaborator
Shiraz University of Medical Sciences

Country where clinical trial is conducted

Iran, Islamic Republic of, 

See also
  Status Clinical Trial Phase
Completed NCT02566733 - Minto Model in Effect Site Mode for Target-Controlled Infusion of Remifentanil During Cardiopulmonary Bypass Phase 4
Completed NCT05601674 - The Effect of Low Flow Anesthesia on Postoperative Emergence Agitation in Rhinoplasty N/A
Completed NCT04634721 - Transversus Abdominis Plan Block, Ultrasound or Laparoscopic? N/A
Completed NCT01873612 - Acute Ventilatory Response to Hypoxia During Sedation With Dexmedetomidine Compared to Propofol in Healthy Male Volunteers Phase 4
Not yet recruiting NCT06462196 - Natural History of Depression, Bipolar Disorder and Suicide Risk
Not yet recruiting NCT05406102 - Remimazolam Improves the Safety in Elderly Patients Undergoing Gastrointestinal Endoscopy Phase 4
Recruiting NCT05700214 - Lidocaine Versus ESP - After Bariatric Surgery N/A
Recruiting NCT04124757 - Impact of Deep Versus Standard Muscle Relaxation on Intra-operative Safety N/A
Completed NCT04699500 - Spanish Validation and Cross-cultural Adaptation of the QoR-15E
Completed NCT03817359 - Use of a Remifentanil-propofol Mixture in Patients Undergoing Breast Cancer Surgery N/A