Actively Recruiting
Incidence of Residual Neuromuscular Blockade in Patients With Frailty Undergoing Gynecologic Cancer Surgery
Led by Mahidol University · Updated on 2025-05-08
622
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to understand how frailty affects patients undergoing gynecologic cancer surgery, including vulvar, endometrial, and ovarian cancers. Frailty is linked with higher risks of complications, longer hospital stays, and increased mortality. The study specifically investigates how leftover neuromuscular blocking drugs after surgery relate to frailty in these patients, a connection not previously studied in gynecologic oncology. Participants will receive a nerve stimulation test called Train of Four (TOF) using specialized equipment in the recovery room after surgery to detect residual muscle relaxants. The study will observe these patients from just before surgery up to a year after, collecting data on the presence of frailty, anesthesia methods, blood transfusions, use of blood pressure medications, and various postoperative outcomes including complications and mortality. Throughout the study, patients will be monitored closely with assessments of neuromuscular blockade within 30 minutes after surgery and frailty checks within 24 hours before surgery. Researchers will track hospital stay length, intensive care admissions, mechanical ventilation use, and pulmonary issues up to 30 days post-operation. This comprehensive follow-up will help clarify how frailty and residual muscle relaxants impact recovery and prognosis after gynecologic cancer surgery.
CONDITIONS
Brief Title
Incidence of Residual Neuromuscular Blockade in Fraility in OncoGynae Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age >= 18 years
- Patients undergoing elective gynecologic-oncology surgery
You will not qualify if you...
- Unable to communicate in Thai
- Unable to understand the questionnaire
- Preexisting neuromuscular disease
- Preexisting wrist disease that may affect nerve stimulator examination
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Within 30 minutes after surgery
Participants undergo nerve stimulation using a Train of Four (TOF) nerve stimulator in the recovery room after surgery to assess residual neuromuscular blockade.
1 visit (in-person) in the recovery room
Duration - Up to 1 year after surgery
Participants are monitored for postoperative outcomes including length of hospital stay, intensive care unit admission, pulmonary complications, and mortality over the following days to one year.
Follow-up visits as per routine postoperative care
Trial Site Locations
Total: 1 location
1
Anesthesiology department, Siriraj hospital, Mahidol University
Bangkok, Bangkok, Thailand, 10700
Actively Recruiting
Research Team
P
Patchareya Nivatpumin, M.D.
J
Jitsupa Nithiuthai, M.D.
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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