Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00226876
Other study ID # 2005/016
Secondary ID
Status Completed
Phase N/A
First received September 26, 2005
Last updated May 28, 2013
Start date February 2005
Est. completion date March 2006

Study information

Verified date September 2005
Source Melbourne Health
Contact n/a
Is FDA regulated No
Health authority Australia: Department of Health and Ageing Therapeutic Goods Administration
Study type Observational

Clinical Trial Summary

Patients commonly report that they have been dreaming when they awaken from general anaesthesia. Our hypothesis is that patients who report dreaming are less deeply anaesthetised during anaesthesia than patients who do not report dreaming. Depth of anaesthesia will be determined using a processed electroencephalographic monitor (called the BIS monitor).


Description:

In this study, we will record the depth of anaesthesia during surgery with the BIS monitor and then interview patients immediately upon emergence to determine whether they recall dreaming or not. The depth of anaesthesia of dreamers and non-dreamers will be assessed.


Recruitment information / eligibility

Status Completed
Enrollment 300
Est. completion date March 2006
Est. primary completion date March 2006
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Age 18-50 years

- American Society of Anesthesiologists physical status 1-3

- Non-cardiac surgery under relaxant general anaesthesia

- Tracheal extubation planned at end of surgery

Exclusion Criteria:

- Inadequate English language skills (due to language barrier, cognitive deficit or intellectual disability)

- Major drug abuse or psychiatric condition

- Expected to be unable to co-operate or be available for followup

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Australia Royal Melbourne Hospital Melbourne Victoria
Australia King Edward Memorial Hospital for Women Perth Western Australia
Australia Royal Perth Hospital Perth Western Australia

Sponsors (2)

Lead Sponsor Collaborator
Melbourne Health Australian and New Zealand College of Anaesthetists

Country where clinical trial is conducted

Australia, 

See also
  Status Clinical Trial Phase
Completed NCT04579354 - Virtual Reality (VR) Tour to Reduce Preoperative Anxiety Before Anaesthesia N/A
Completed NCT02920749 - Study of Anaesthesia Costs and Recovery Profiles N/A
Active, not recruiting NCT02184780 - Impact of Perinatal Anaesthesia and Analgesia on Neurocognitive Outcomes in Early Childhood
Completed NCT02025153 - Comprehensive Pain Programme to Determine Mechanism of Transition of Acute to Chronic Postsurgical Pain N/A
Completed NCT02265822 - Melatonin Premedication in Children Undergoing Surgery Phase 4
Completed NCT01457274 - "Light" Versus "Deep" Bispectral Index (BIS) Guided Sedation for Colonoscopy N/A
Completed NCT00521612 - Sevoflurane vs. Isoflurane for Low-Flow General Anaesthesia for Abdominal Surgery N/A
Completed NCT00455117 - Effect of Parecoxib on Post-craniotomy Pain Phase 4
Completed NCT02150460 - A Comparison of One-site and Two-site Peribulbar Anaesthesia for Cataract Surgery at Kaduna, Nigeria Phase 4
Completed NCT01041352 - Laryngeal Mask or Endotracheal Tube for Back Surgery in the Prone Position N/A
Terminated NCT02801799 - Effects of Local Anaesthetic Infusion Rates on Nerve Block Duration Phase 1
Completed NCT02923427 - I-gel vs LMA Supreme in Laparoscopic Gynecological Surgery N/A
Completed NCT01971996 - Measuring the Effect of External Pressure on the Regional Cerebral Oxygen Saturation Monitored by Near-infrared Spectroscopy(NIRS) Technology N/A
Completed NCT01076790 - Dexmedetomidine-propofol-remifentanil Anaesthesia and Reactivity to Noxious Stimuli Phase 4
Completed NCT01022151 - Aminophylline and Cognitive Function After Sevoflurane Anaesthesia Phase 2
Completed NCT02442609 - Internet for Anesthesia Information : a Patient Questionaire N/A
Recruiting NCT02125838 - Laryngeal Mask Supreme During Laparoscopic Gynecologic Surgery Phase 4
Completed NCT01780571 - CPAP/PSV Preoxygenation in Obese Patients N/A
Completed NCT03380715 - A Comparison Between Co-phenylcaine Nasal Spray and Nasal Nebulization Prior to Rigid Nasoendoscopic Examination N/A
Recruiting NCT04070404 - Quality of Preoxygenation in Emergency Surgery