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Comparison of Opioid Based and Opioid Free Anaesthesia in Transsphenoidal Surgery

Comparison of Opioid Based and Opioid Free Anaesthesia in Transsphenoidal Surgery for Haemodynamic Stability and Recovery Characteristics

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03120234
Enrollment
60
Registered
2017-04-19
Start date
2017-01-31
Completion date
2017-12-31
Last updated
2019-07-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Opioid Free Anaesthesia

Brief summary

This study has been planned to compare the effect of opioid free anaesthesia using dexmedetomidine and ketamine with opioid based anaesthesia using fentanyl in maintaining the intraoperative hemodynamic stability and recovery characteristics in patients undergoing Transsphenoidal surgery of pituitary tumors.

Detailed description

Opioid Free Anesthesia (OFA) is a technique where no intraoperative opioid is administered during the anesthetic management. Opioid free anesthesia is usually achieved through sympatholysis, analgesia, and anesthesia with dexmedetomidine and analgesia with low dose ketamine. In addition paracetamol and other non-steroidal anti inflammatory drugs (NSAIDS) may be used as adjuncts to the multi-modal pain regimen. Dexmedetomidine, a highly selective agonist of the alpha2 adrenergic receptor, has many clinical benefits, such as sedation, analgesia, preventing unwanted stress responses and low risk of respiratory depression. Because of concern that opioids might cause perioperative respiratory depression, substitution with dexmedetomidine will be helpful with its analgesic and sympatholytic properties. Dexmedetomidine has shown to reduce minimum alveolar concentration (MAC) of inhalational anesthetics and the requirement of perioperative opioid by 30-50%. In neurosurgical patients, dexmedetomidine is helpful in maintaining intracranial pressure (ICP) and intraoperative hemodynamic stability, especially during intubation and extubation. It can allow for faster awakening and thus an earlier neurological examination by decreasing necessary volatile agent and opioid doses. Ketamine, an N-methyl-d-aspartate(NMDA) antagonist, blunts central pain sensitization at sub-anesthetic doses (0.5 mg/kg or less) and has been studied extensively as an adjunct for perioperative analgesia. Sub-anesthetic ketamine improves pain scores and reduces perioperative opioid consumption in a broad range of surgical procedures.Recent literature has suggested that adjuvant ketamine administration in mechanically ventilated patients has no cerebrovascular effects. The present study has been planned to compare the effect of opioid free anesthesia using dexmedetomidine and ketamine with opioid based anesthesia using fentanyl in maintaining the intraoperative hemodynamic stability and recovery characteristics in patients undergoing TSS of pituitary tumors.

Interventions

DRUGDexmedetomidine
DRUGKetamine
DRUGFentanyl
DRUGPlacebos

o.9% normal saline will be used instead of ketamine

Sponsors

Post Graduate Institute of Medical Education and Research, Chandigarh
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* patients suffering significant pituitary adenocarcinomas posted for transsphenoidal resection of tumor * age group between 18 to 65 yr * Both males and females * ASA physical status 1 to 2

Exclusion criteria

* pts taking opioid for chronic pain * Pregnant or nursing woman * Preoperative GCS \<15 * HR\<50/min * Patients with allergies to study medication * Patients with psychiatric disorder * Patients with unstable cardiorespiratory disorder * Patients with hepatic and renal insufficiency

Design outcomes

Primary

MeasureTime frameDescription
to measure the level of cognition in both the groups15minusing Short orientation memory concentration test (SOMC test)
To measure the emerence and extubation times in both groups15minutesit is measured by noting the time for emergence and extubation after stopping inhalational anaesthesia.
to measure the level of emergence in both the groups15minusing Riker sedation-agitation score

Secondary

MeasureTime frameDescription
comparison of intraoperative hemodynamic stability in both the groupsintra operative periodthis will be done by monitoring intraoperative hemodynamics and noting down no of events of hypotension and hypertension and noting down the rescue drug requirements.
postoperative pain assessment by using numeric rating scale24 hrs
comparing postoperative analgesic dose requirement in both the groups24hrs

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026