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A study to assess the rate of occurence of nausea and vomiting followed by the addition of the drug morphine given as apart of anaesthesia for patients with carcinoma cervix undergoing high dose (HDR) intracavitary brachytherapy.

Not Applicable
Conditions
Health Condition 1: C539- Malignant neoplasm of cervix uteri, unspecified
Registration Number
CTRI/2020/06/025687
Lead Sponsor
Christian MedicalCollegeVellore
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
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

pain

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

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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