Clinical Trials Directory

Trials / Unknown

UnknownNCT03132259

Comparative Low and High Dose of Dexmedethomidine in Pituitary Tumor Removal by Transphenoid Approach

Comparative Low and High Dose of Dexmedethomidine Can Stabilize Hemodynamics and Blood Loss in Pituitary Tumor Removal by Transphenoid Approach

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
124 (estimated)
Sponsor
Mahidol University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

Transnasal transsphenoidal (TNTS) resection of pituitary tumors involves wide fluctuation in hemodynamic parameter and causes hypertension and tachycardia due to intense noxious stimuli during various stages of surgery. None of routinely used anesthetic agents effectively blunts the undesirable hemodynamic responses, and therefore usually there is a need to use increased doses of anesthetic agents. Dexmedetomidine (DEX) an α-2 adrenergic receptor agonist, because its sympatholytic and antinociceptive properties may ensure optimal intraoperative hemodynamic stability during critical moments of surgical manipulation. In addition, DEX reduced the anesthetic requirement with rapid recovery at the end of surgery. The main aim of the study was to evaluate the effect of DEX on perioperative hemodynamics, anesthetic requirements

Detailed description

DEX as an anesthetic adjuvant improved hemodynamic stability and decreased anesthetic requirements in patients undergoing TNTS resection of pituitary tumor. In addition, DEX provided better surgical field exposure conditions and early recovery from anesthesia

Conditions

Interventions

TypeNameDescription
DRUGhigh dose dexmedethomidineDexmedethomidine continuous drip 0.5 mcg/kg/hr a
DRUGlow dose dexmedethomidineDexmedethomidine continuous drip 0.2 mcg/kg/hr

Timeline

Start date
2016-05-01
Primary completion
2017-05-01
Completion
2018-06-01
First posted
2017-04-27
Last updated
2017-05-30

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT03132259. Inclusion in this directory is not an endorsement.