Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
ID06216002

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

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Age >= 18 years
  • Patients undergoing elective gynecologic-oncology surgery
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

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

Long-term Monitoring

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

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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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