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Clinical Trials/CTRI/2020/06/025687
CTRI/2020/06/025687
Not yet recruiting
未知

Prospective observational study to assess the incidence of nausea and vomiting following intrathecal morphine given as apart of anaesthesia for patients with carcinoma cervix undergoing high dose rate (HDR) intracavitary brachytherapy.

Christian MedicalCollegeVellore0 sites0 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: C539- Malignant neoplasm of cervix uteri, unspecified
Sponsor
Christian MedicalCollegeVellore
Status
Not yet recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Observational

Investigators

Sponsor
Christian MedicalCollegeVellore

Eligibility Criteria

Inclusion Criteria

  • 1\) Histologically proven carcinoma cervix for
  • intracavitary brachytherapy.
  • 2\) ASA I/II
  • 3\) Consent for participation in study

Exclusion Criteria

  • 1\) Patient undergoing treatment for chronic
  • 2\) Preoperative history of nausea and vomiting
  • requiring treatment
  • 3\) Unfit for spinal anaesthesia like
  • Coagulopathy, cardiac lesions, infection at
  • the site of spinal injection, fever
  • 4\) Unwilling or unable to give consent

Outcomes

Primary Outcomes

Not specified

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