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NOT YET RECRUITING
NCT06281561
PHASE3

Dexmedetomidine Premedication for Post-anaesthesia Sleep Disturbance

Sponsor: The First Affiliated Hospital of Xiamen University

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is to learn about the effect of preoperative nasal spry with dexmedetomidine on postoperative sleep disturbance in young to middle-aged women undergoing hysteroscopy. The main questions it aims to answer are:1) what is the incidence of postoperative sleep disturbance in unisex patients who receive propofol anesthesia. 2) The preventive effect of preanesthesia nasal spray dexmedetomidine on postoperative sleep disturbance. Participants will receive total intravenous propofol anaesthesia after dexmedetomidine nasal spray. Sleep quality will be monitored by using a Wearable devices and the PSQI which was used to assess sleep quality 1,2 days before the surgery and 1,3,7 days after surgery. Researchers will compare the effects of 0.2 or 0.5 ug/kg dexmedetomidine to see if it help improve postanesthesia sleep quality.

Official title: Effect of Intranasal Dexmedetomidine Premedication on Sleep Disturbance After General Anaesthesia

Key Details

Gender

FEMALE

Age Range

23 Years - 45 Years

Study Type

INTERVENTIONAL

Enrollment

110

Start Date

2024-05-01

Completion Date

2024-12-31

Last Updated

2024-04-16

Healthy Volunteers

Yes

Interventions

DRUG

Normal Saline

Female patients undergoing hysteroscopy receive nasal spray with normal saline before anesthesia

DRUG

Dexmedetomidine

Female patients undergoing hysteroscopy receive nasal spray with dexmedetomidine before anesthesia