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NCT05005715

Effect of Dexmedetomidine on Quality of Recovery in Non-functioning Pituitary Adenoma Patients Undergoing Endoscopic Transsphenoidal Surgery

Status unknown Phase 2 Last updated 13 August 2021
What this trial tests

Phase 2 trial testing Dexmedetomidine in Non-functioning Pituitary Adenoma in 64 participants. Status unknown.

Timeline
30 August 2021
Primary endpoint
29 August 2022
29 August 2023

Quick facts

Lead sponsorSeoul National University Hospital
PhasePhase 2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposehealth services research
Enrollment64
Start date30 August 2021
Primary completion29 August 2022
Estimated completion29 August 2023
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Seoul National University Hospital

Who can join

Adults 20 to 65, any sex, with Non-functioning Pituitary Adenoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In multiple previous studies that have explored the use of dexmedetomidine in transsphenoidal tumor resection surgery, dexmedetomidine showed many beneficial effects like reducing the requirement of analgesics and anesthetics, improving hemodynamic stability and decreasing the emergence time, extubation time and visual analog scale at emergence. Therefore, the investigators hypothesized that dexmedetomidine would decrease neuroendocrine stress response and improve the quality of postoperative recovery.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Dexmedetomidine

Trials testing the same drug.

Other recruiting trials for Non-functioning Pituitary Adenoma

Currently open trials in the same condition.

Other Seoul National University Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05005715.

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