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To determine the efficacy between time dependent vs volume dependent chest tube drainage removal protocol following talc slurry pleurodesis in malignant pleural effusion - A randomized control trial

Phase 1
Not yet recruiting
Conditions
Health Condition 1: C00-D49- Neoplasms
Registration Number
CTRI/2020/07/026652
Lead Sponsor
Christian Medical College
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Age more than 18 years with biopsy/cytology proven malignant pleural effusion and planned for TALC pleurodesis

Exclusion Criteria

1.Patients who do not give informed consent

2.Expected survival period of less than 2 months

3.Patient with earlier pleurodesis failure

4.Evidence of trapped lung following drainage of pleural fluid- Trapped lung defined as evidence of failed re-expansion of the lung after pleural fluid drainage and confirmed by chest X-ray

5.Ipsilateral endobronchial obstruction

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Efficacy of Pleurodesis in two different chest drain removal protocols (volume versus time based chest drain removal protocols)Timepoint: Sucess of pleurodesis will be assessed at the end of 7days, 1month and 3 months.
Secondary Outcome Measures
NameTimeMethod
To compare complications and Mortality in two arms <br/ ><br>Timepoint: Complications and mortailty will be assessed at the end of 7days, 1month and 3 months.;To compare the duration of hospital stay in two arms following talc pleurodesisTimepoint: Will be assessed only once at the end of hospital stay
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