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se of ultrasound in prostate surgeries to estimate fluid balance

Not Applicable
Conditions
Health Condition 1: N401- Benign prostatic hyperplasia withlower urinary tract symptoms
Registration Number
CTRI/2023/11/059619
Lead Sponsor
Jenifer A
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

All patients of ASA grade 1,2,3 between the age of 40 to 80 years who are undergoing endoscopic prostate surgeries and willing to participate in the study

Exclusion Criteria

1.Patients not willing to participate in the study

2.Patients with Parotitis,Sialdenitis

3.Patients with Mumps,Sjogrens disease

4.Patients with tumours of Parotid gland

5.Patients with autoimmune diseases,ASA 4 and 5

6.Patients who have undergone radiotherapy for head and neck malignancies

7.All the patients will be explained about the study and the need to shave for the study.If they are not willing to shave for religious reasons or personal discomfort,they will be excluded from the study

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To detect parotid gland enlargement by ultrasound which occurs as a result of excessive fluid absorption during endoscopic prostate surgeriesTimepoint: Till 1 hour post surgery
Secondary Outcome Measures
NameTimeMethod
1.To detect fluid overload occuring in endoscopic prostate surgeries <br/ ><br>2.To detect dilutional hyponatremiaTimepoint: Till 24 hours post surgery
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