Comparison of Neuroprotection by Propofol and Desflurane for POCD Following Subarachnoid Hemorrhage Surgery

Sponsor
Postgraduate Institute of Medical Education and Research (Other)
Overall Status
Completed
CT.gov ID
NCT02987218
Collaborator
(none)
100
1
2
16.1
6.2

Study Details

Study Description

Brief Summary

Aneurysmal subarachnoid hemorrhage (aSAH) is characterized by the rupture of an intracranial aneurysm and accumulation of blood in the subarachnoid space with 30 to 40% mortality rate. Amongst the survivors 40-50% suffers disability due to cognitive decline.Trends towards early surgery offers challenge to anesthesiologist to provide optimum brain relaxation and simultaneously maintaining stable hemodynamics. Anesthetic agents are administered to conduct smooth neurosurgical procedure. These agents may affect patient's cognitive function postoperatively.Currently most common anesthetic agents used are either intravenous hypnotic agents (propofol) or volatile inhalational agents (isoflurane/sevoflurane/desflurane). Provision of neuroprotection with propofol and volatile inhalational agents has been studied by various authors.Not many studies have been performed in patients undergoing aneurysmal clipping surgeries looking into effects of various anesthetic agents on intraoperative (I/O) brain condition, I/O hemodynamic and POCD.Thus present study is planned to compare propofol and desflurane for long term postoperative cognitive decline in patients undergoing surgery following aneurysmal subarachnoid hemorrhage.

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

100 patients will be randomized into two groups, Desflurane group (Group D) and Propofol group (Group P) using a computer generated algorithm. Written informed consent will be taken from all the patients.

Cognition assessed using MOCA (Montreal Cognitive Assessment)test. A preoperative assessment for establishing the patient's baseline performance. Surgery-related factors may affect test performance if performed too early to reduce possibility of confounding factors, we planned to conduct the test for POCD at the time of discharge of the patient after surgery. To compare long term protection provided by anesthetic agent cognitive functions were assessed at one month following surgery.

Cognitive functions will be assessed at following time period A) Preoperatively B) Postoperatively B1- At the time of discharge B2- 1month after discharge following surgery.

Biomarker levels S100B levels were also measured A) Preoperatively B) Intraoperatively - post clipping C) Postoperatively - 1hour after surgery

Study Design

Study Type:
Interventional
Actual Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Comparison Of Pharmacological Neuroprotection Provided By PROPOFOL VERSUS DESFLURANE For Long Term Postoperative Cognitive Dysfunction In Patients Undergoing Surgery For Aneurysmal Subarachnoid Hemorrhage
Study Start Date :
Jul 1, 2015
Actual Primary Completion Date :
Oct 1, 2016
Actual Study Completion Date :
Nov 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: PROPOFOL

Intravenous hypnotic agent Decrease Cerebral Metabolic reduction Decrease ICP(Intracranial pressure) Better cognitive Function preservation

Drug: Propofol
Intravenous hypnotic agent Decrease Cerebral Metabolic reduction Decrease ICP Better cognitive Function preservation

Active Comparator: DESFLURANE

Inhalational agent. Decreases cerebral metabolism Increase /decreases ICP Cognition preservation

Drug: Desflurane
Inhalational agent. Decreases cerebral metabolism Increase /decreases ICP Cognition preservation

Outcome Measures

Primary Outcome Measures

  1. Assessment of cognitive function at one month following surgery. [One month]

    Montreal Cognitive Assessment scale is used

Secondary Outcome Measures

  1. Assessment of cognitive function preoperatively Assessment of cognitive function at discharge. Comparison of biomarker of cognitive dysfunction [Baseline cognition assessment prior to surgery]

    Montreal Cognitive Assessment scale used

  2. Assessment of cognitive function preoperatively Assessment of cognitive function at the time of discharge from hospital [Discharge from hospital]

    Montreal Cognitive Assessment scale used

  3. Comparison of biomarker (S-100B) levels [Prior to surgery , After clipping of aneurysm, One hour after completion of surgery]

    Blood sample for S100B levels used

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Patients scheduled for aneurysmal SAH surgery with clinical and radiological evidence of cerebral aneurysm.

  2. Age between 18 to 65 yrs.

  3. World Federation of neurosurgery grade 1, 2.

  4. American society of Anesthesia grade 1, 2 and 3.

Exclusion Criteria:
  1. Co-morbidities other than hypertension and diabetes mellitus like cardiovascular disease and respiratory impairment.

  2. Patients with known psychiatric disease.

  3. History of drug abuse.

  4. Low level of education (illiterate) or multiple failures in school.

  5. Patients who are unconscious, intubated or tracheostomised even after two weeks following exposure to anesthesia will also be excluded from the study.

  6. Intraoperative complications like massive blood loss, prolonged clipping time(>20minutes), severe intraoperative brain swelling precluding replacement of bone flap.

  7. Patients with infectious diseases and respiratory complications.

  8. Multiple surgeries.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Postgraduate institute of medical education and research Chandigarh India 160012

Sponsors and Collaborators

  • Postgraduate Institute of Medical Education and Research

Investigators

  • Principal Investigator: Shalvi Mahajan, MD, Postgraduate Institute of Medical Education and Research
  • Principal Investigator: Hemant Bhagat, DM, Postgraduate Institute of Medical Education and Research

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dr Shalvi mahajan, Senior Resident, Postgraduate Institute of Medical Education and Research
ClinicalTrials.gov Identifier:
NCT02987218
Other Study ID Numbers:
  • INT/IEC/2015/741
First Posted:
Dec 8, 2016
Last Update Posted:
Dec 8, 2016
Last Verified:
Dec 1, 2016
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Keywords provided by Dr Shalvi mahajan, Senior Resident, Postgraduate Institute of Medical Education and Research
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 8, 2016