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RECRUITING
NCT05978505
PHASE2

Reboxetine for Sleep Apnoea After ENT Surgery

Sponsor: Flinders University

View on ClinicalTrials.gov

Summary

This pilot study will establish the feasibility of a larger trial to investigate whether reboxetine, a medication used to treat depression, can reduce the severity of obstructive sleep apnea (OSA) including increased blood oxygenation in post-surgical OSA patients where positive airway pressure (CPAP) therapy is either frequently poorly tolerated or not an option immediately post surgery. In this randomized, placebo-controlled, double-blind study, participants will use at-home sleep monitoring equipment before and after surgery plus measures of oxygenation. They will be prescribed either reboxetine or a placebo for seven days after surgery and complete questionnaires at the beginning and end of the study.

Official title: Reboxetine for Obstructive Sleep Apnoea After Upper Airway Surgery: a Randomised, Double-blind, Placebo-controlled Study

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

20

Start Date

2023-08-10

Completion Date

2025-07

Last Updated

2024-10-03

Healthy Volunteers

No

Interventions

DRUG

Reboxetine 4 MG Oral Tablet

7 nightly doses (4mg) to commence after surgery.

DRUG

Placebo

7 nightly doses to commence after surgery.

Locations (1)

Flinders, Private and Public Hospitals and Flinders University

Bedford Park, South Australia, Australia