MedPath

Efficacy & Safety of Pigtail Catheter Drainage Versus Need Based Thoracocentesis for Recurrent Hepatic Hydrothorax.

Not Applicable
Not yet recruiting
Conditions
Hepatic Hydrothorax
Interventions
Procedure: Pigtail Catheter
Procedure: Large Volume Thoracocentesis
Registration Number
NCT06007820
Lead Sponsor
Institute of Liver and Biliary Sciences, India
Brief Summary

In cirrhotic patients with recurrent hepatic hydrothorax liver transplantation is a definitive treatment. But a significant number of individual are ineligible for liver transplantation. In these patients to ameliorate the symptoms various treatment modalities such as TIPS, serial thoracocentesis, pigtail catheter drainage and pleurodesis are used. We are doing this study to assess the safety and efficacy of serial thoracocentesis verus pigtail catheter drainage.

Detailed Description

* Study population - Cirrhotic patients with recurrent hepatic hydrothorax

* Study design - A prospective, randomized, single center open label study

* Block Randomization, block size - 10

* Sample size - Assuming in single time thoracocentesis group 5+/-3.67 thoracocentesis is required, investigator expect a 50 % reduction in pigtail drainage group. Apha error- 5, power -90, 15% dropout 35 patients in each arm

* Intervention - Group 1 - on-demand therapeutic thoracocentensis, Group 2 - small volume frequent thoracocentesis using PCD.

* Monitoring and assessment

* At enrollment:

(A) Complete history and examination

1. Etiology of cirrhosis

2. Severity of ascites, Jaundice

3. Prior Hepatic encephalopathy, bleed, Jaundice

4. Prior Spontaneous bacterial peritonitis, large volume paracentesis frequency

5. Pattern and number of prior decompensation

6. Prior Acute on Chronic Liver Failure and Acute Kidney episodes

7. Use of non selective beta blockers, norfloxaxin, rifaximin and albumin

8. History of Endoscopic Variceal ligation or other endotherapy

9. History of Hypertension, Diabetes

10. Fever , signs of sepsis (SIRS)

11. Examination- Sarcopenia, fraility, icterus, pedal edema

At follow-up (at daily till Day - 7, thereafter at Day - 30 and Day 90) Complete history and examination

1. Complications - SBP, SBE, ACLF and Jaundice, HE/ AKI episodes

2. HTN, Diabetes control

3. Fever , signs of sepsis (SIRS)

4. Examination- Sarcopenia, fraility, icterus, pedal edema, ascites, HE Clinical Evaluation

1. Etiology of chronic liver disease (Baseline) 2. Severity of liver disease (Baseline, Day - 7, Day - 30, Day - 90 ) 3. MELD score, MELD-Na score, CTP score (Baseline, Day - 7, Day - 30, Day - 90 ) 4. Complications (Baseline, Day - 7, Day - 30, Day - 90 ) 5. Overt HE, PHT related Bleed, clinical jaundice, ascites, hyponatremia, AKI, SBP, Infection (specify site and severity), Frequency of Large Volume Paracentesis, On Demand Thoracocentesis

* Labs and follow up Baseline (at admission) -

1. Blood : KFT, LFT, CBC, INR, AFP, PCT, S.PRA, Pro-BNP, Urinary Na

2. Imaging : USG abdomen, X-ray chest, 2D ECHO

3. Pleural fluid/ ascitic fluid - TLC, DLC, Protein, Sugar, SPAG, SAAG, ADA, c/s

4. Hemodynamics : Intrapleural pressures at first TT

5. Baseline (at randomization, Day -3 and Day - 7 in PCD-TT) -

6. Blood : KFT, INR; S.PRA, Pro-BNP, Urinary Na (at Day 7)

7. Imaging : X-ray chest

8. Pleural fluid/ ascitic fluid - TLC, DLC, SPAG, c/s if indicated

9. Day - 60, Day - 90 (end of follow-up)

10. Blood : KFT, LFT, CBC, INR, AFP

11. Imaging : USG abdomen, X-ray chest, 2D ECHO

* STATISTICAL ANALYSIS -

1. Data will be reported as mean + SD.

2. Categorical variables will be compared using the chi-square test or Fisher exact test

3. Normal continuous variables will be compared using the Student's t test

4. Non normal continuous variables will be compared using the Mann-Whitney rank-sum test (unpaired data) or the Wilcoxon test (paired data).

5. The actuarial probability of survival will be calculated by the Kaplan-Meier method and compared using the log-rank test.

6. A Cox regression analysis will be performed to identify independent prognostic factors for survival.

7. Univariate and multivariate analysis will be used whenever applicable.

* Adverse effects - Chest pain, pain at the site, Breathlessness, infection, pneumothorax, infection, bleeding

* Stopping rule -

1. Liver Transplant

2. Appearance of SBP, PICD, HE.

3. Mortality

4. End of follow-up

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
70
Inclusion Criteria
  1. Age 18-75 years
  2. CLD with refilling symptomatic hepatic hydrothorax
Exclusion Criteria
  1. CTP >12, MELD>25
  2. Tubercular PE, Ischemic cardiac disease
  3. If opting for TIPS/ LT
  4. Severe HPS
  5. Prior or current SBE/ SBP, septic shock
  6. Patients on mechanical ventilator
  7. Serum Creatinine >2 mg/dl
  8. Extrahepatic malignancy
  9. Serum Sodium < 120
  10. Post TIPS/ BRTO/ SAE patients
  11. Post renal or liver transplantation
  12. Lack of informed consent
  13. Hepatocellular carcinoma outside milan criteria
  14. Non-cirrhotic portal HT
  15. Known HIV infection
  16. Pregnant women

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Pigtail CatheterPigtail CatheterGroup 2 - small volume frequent thoracocentesis using PCD
Large Volume ThoracocentesisLarge Volume ThoracocentesisGroup 1 - on-demand therapeutic thoracocentensis
Primary Outcome Measures
NameTimeMethod
Frequency of Repeated ThoracocentesisDay 90
Secondary Outcome Measures
NameTimeMethod
Hepatic encephalopathy: Grading as per West Haven Classification.Day 90

West Haven Grade (1-4) will be used to assess Hepatic Encephaloapthy, Grade 4 means worse outcome.

Change in Renal parameters - Serum Creatinine at Day 90Day 90
Proportion of participants developing Na < 120 meg/l Day 7Day 7
Proportion of patients developing Spontaneous Bacterial Empyema Day 90Day 90
No. of days pateint surviving without Liver transplant and TIPS at Day 7Day 7
Frequency of Repeated Thoracocentesis.Day 30 and Day 90
Number of times Thoracocentesis is required between both groups at Day 30Day 30
Change in Renal parameters - Serum Creatinine at Day 7Day 7
Change in Renal parameters - Serum Creatinine at Day 30Day 30
Dose of Diuretic in each arm Day 30Day 30
Proportion of patient developing Spontaneous Bacterial Peritonitis at Day 90Day 90
Incidence of refilling hydrothorax within72 hours
Number of times Thoracocentesis is required between both groups at Day 90Day 90
Proportion of pateint developing Post thoracocentesis Shock (Change in Heart Rate, Blood pressure) at Day 7Day 7
Rate of Complete Response, Partial Response, No response.Day 7, Day 30, Day 90
Proportion of participants developing Na < 120 meg/l Day 30Day 30
Proportion of patients developing Spontaneous Bacterial Empyema Day 7Day 7
Proportion of pateint developing Post thoracocentesis Shock (Change in Heart Rate, Blood pressure) at Day 30Day 30
Proportion of pateint developing Post thoracocentesis Shock (Change in Heart Rate, Blood pressure) at Day 90Day 90
Proportion of patients developing Spontaneous Bacterial Empyema Day 30Day 30
No. of days pateint surviving without Liver transplant and TIPS at Day 90Day 90
No. of days pateint surviving without Liver transplant and TIPS at Day 30Day 30
Proportion of participants developing Na < 120 meg/l Day 90Day 90
Dose of Diuretic in each arm Day 7Day 7
Dose of Diuretic in each arm Day 90Day 90
Incidence of Post procedure complications in between both groups at Day 90Day 90
Proportion of patient developing Spontaneous Bacterial Peritonitis at Day 7Day 7
Proportion of patient developing Spontaneous Bacterial Peritonitis at Day 30Day 30
Incidence of Post procedure complications in between both groups at Day 30Day 30
Changes in CTP between the groupsDay 90
Number of Episodes of Hospitalization between both groups at Day 7Day 7
Number of Episodes of Hospitalization between both groups at Day 90Day 90
Incidence of Post procedure complications in between both groups at Day 7Day 7
Number of Episodes of Hospitalization between both groups at Day 30Day 30
Cumulative dose of albumin at D7 in two groupsDay 7
Cumulative dose of albumin at D30 in two groupsDay 30
Cumulative dose of albumin at D90 in two groupsDay 90
Changes in MELD between the groupsDay 90

Trial Locations

Locations (1)

Institute of Liver & Biliary Sciences

🇮🇳

New Delhi, Delhi, India

© Copyright 2025. All Rights Reserved by MedPath