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Comparison of Dexamethasone and N Acetylcysteine (NAC) Versus N Acetylcysteine (NAC) Alone in the Prevention of Post Embolization Syndrome in Patients With Hepatocellular Carcinoma Following Transarterial Chemoembolization.

Primary Purpose

Hepatocellular Carcinoma

Status
Not yet recruiting
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
N Acetylcysteine
Dexamethasone
Placebo
Sponsored by
Institute of Liver and Biliary Sciences, India
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatocellular Carcinoma

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: All patients undergoing TACE procedure Valid Consent Age 18-65 years Exclusion Criteria: Child Pugh C, Child Pugh B > 8 HCC patients with a curative therapy (Ablation, Resection or LT) ECOG Performance Status 3-4 Pregnancy History of allergic reaction from NAC significant cardiopulmonary disease UGI bleed within last 28 days Recent surgery within last 28 days Documented febrile illness in last 1 weeks Uncontrolled Diabetes (FBS > 200, HBA1C > 8) Uncontrolled Hypertension (BP > 160/100) Structural kidney disease with eGFR < 60 ml/min

Sites / Locations

  • Institute of Liver & Biliary Sciences

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

NAC+Dexamethasone

NAC+Placebo

Arm Description

NAC started at 12 hr prior to procedure - (150 mg/kg/hr for 1 hr followed by 12.5 mg/Kg/hr for 4 hr, then continuous infusion of 6.25 mg/h for 48 after the procedure. Dexamethasone 20 mg in 5 ml NS 1 hour prior to procedure and 8 mg in 5 ml NS at day 2, day 3. Placebo 5 ml NS 1 hr prior to procedure.

NAC started at 12 hr prior to procedure - (150 mg/kg/hr for 1 hr followed by 12.5 mg/Kg/hr for 4 hr, then continuous infusion of 6.25 mg/h for 48 after the procedure.

Outcomes

Primary Outcome Measures

Prevention of post-embolization syndrome
Prevention of Post-embolization syndrome , Defined base on South west oncology group (SWOG) toxic coding less than 2 score

Secondary Outcome Measures

Prevention of post TACE decompensation at 4 weeks
Metric / Method of measurement : Post TACE decompensation defined as an increase in Child-Pugh score of more than two points or newly developed decompensating events, such as ascites, hepatic encephalopathy, or serum total bilirubin > 2 mg/dL.
Decrease in the duration of hospitalisation
Adverse events of Dexamethasone and NAC in patients undergoing transarterial chemoembolisation for HCC

Full Information

First Posted
August 4, 2023
Last Updated
September 8, 2023
Sponsor
Institute of Liver and Biliary Sciences, India
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1. Study Identification

Unique Protocol Identification Number
NCT06039280
Brief Title
Comparison of Dexamethasone and N Acetylcysteine (NAC) Versus N Acetylcysteine (NAC) Alone in the Prevention of Post Embolization Syndrome in Patients With Hepatocellular Carcinoma Following Transarterial Chemoembolization.
Official Title
Comparison of Dexamethasone and N Acetylcysteine (NAC) Versus N Acetylcysteine (NAC) Alone in the Prevention of Post Embolization Syndrome in Patients With Hepatocellular Carcinoma Following Transarterial Chemoembolization - Randomized Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 15, 2023 (Anticipated)
Primary Completion Date
July 31, 2024 (Anticipated)
Study Completion Date
July 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institute of Liver and Biliary Sciences, India

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
N-acetylcysteine (NAC), a glutathione precursor and potent antioxidant, is known as a liver protector. As a steroid preparation, dexamethasone is known to have efficient anti-inflammation and immunosuppression effects. N-acetyl cysteine and Dexamethasone's roles in preventing post-embolization syndrome following TACE have each been researched individually in the past. Up until now, no study has been done that has compared dexamethasone and NAC in post-embolization syndrome. With this study, we aim to study the efficacy of combining dexamethasone with N-acetyl cysteine in the prevention of post-embolization syndrome within 72 hours among patients who undergo transarterial chemoembolization for HCC.
Detailed Description
Aim & Objectives Hypothesis: The combination of dexamethasone with NAC is superior to NAC alone in prevention of PES among patients who undergo TACE in HCC as both medications work differently to prevent PES. AIM:- To study the efficacy of combining Dexamethasone to N acetyl cysteine in prevention of post embolization syndrome within 72 hours among patients who undergo transarterial chemoembolization for HCC. Objective - PRIMARY Prevention of post embolisation syndrome within 72 hours. SECONDARY Prevention of post embolisation decompensation at 2 weeks. Decrease in the duration of hospitalization. To study the adverse effects of NAC and steroids in patients who undergo transarterial chemoembolisation for HCC. Methodology: Study population: All patients undergoing TACE procedure Valid Consent Age 18-65 years Study design: Monocentric open label prospective randomized controlled study. The study will be conducted in Department of Hepatology, ILBS. Sample size: Assuming that NAC prevents PES by 75% and addition of dexamethasone further prevents PES by 20 % (i.e combination of NAC and Dexamethasone prevents total 95%). Then with alpha as 5% and power 90 % .we need to enroll total 130 cases i.e 65 in each arm. Further assuming 10% drop out , it is decided to enroll 150 cases i.e. 75 in each arm. Allocation will be done randomly by block randomization method, taking block size as 10. Monitoring and assessment: All the parameters of the objective and also noted any adverse effects. Intervention: TACE. STATISTICAL ANALYSIS: The data will be entered in Microsoft excel and will be analyzed using SPSS version 22. The categorical data will be analyzed using Chi square/Fissure test. Exact test and continuous data will be compiled using t-test. Besides this the univariate and multivariate survival analysis will be carried out using Cox regression method. Kaplan-Meier technique will be applied for further analysis. P-value<0.05 will be considered as significant. Adverse effects: allergic drug reaction. Stopping rule: If patient decided to withdraw from study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatocellular Carcinoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
NAC+Dexamethasone
Arm Type
Experimental
Arm Description
NAC started at 12 hr prior to procedure - (150 mg/kg/hr for 1 hr followed by 12.5 mg/Kg/hr for 4 hr, then continuous infusion of 6.25 mg/h for 48 after the procedure. Dexamethasone 20 mg in 5 ml NS 1 hour prior to procedure and 8 mg in 5 ml NS at day 2, day 3. Placebo 5 ml NS 1 hr prior to procedure.
Arm Title
NAC+Placebo
Arm Type
Active Comparator
Arm Description
NAC started at 12 hr prior to procedure - (150 mg/kg/hr for 1 hr followed by 12.5 mg/Kg/hr for 4 hr, then continuous infusion of 6.25 mg/h for 48 after the procedure.
Intervention Type
Drug
Intervention Name(s)
N Acetylcysteine
Intervention Description
NAC started at 12 hr prior to procedure - (150 mg/kg/hr for 1 hr followed by 12.5 mg/Kg/hr for 4 hr, then continuous infusion of 6.25 mg/h for 48 after the procedure.
Intervention Type
Drug
Intervention Name(s)
Dexamethasone
Intervention Description
Dexamethasone 20 mg in 5 ml NS 1 hour prior to procedure and 8 mg in 5 ml NS at day 2, day 3. Placebo 5 ml NS 1 hr prior to procedure.
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
The placebo will be administered in the same way as the drug in the experimental group.
Primary Outcome Measure Information:
Title
Prevention of post-embolization syndrome
Description
Prevention of Post-embolization syndrome , Defined base on South west oncology group (SWOG) toxic coding less than 2 score
Time Frame
72 hours
Secondary Outcome Measure Information:
Title
Prevention of post TACE decompensation at 4 weeks
Description
Metric / Method of measurement : Post TACE decompensation defined as an increase in Child-Pugh score of more than two points or newly developed decompensating events, such as ascites, hepatic encephalopathy, or serum total bilirubin > 2 mg/dL.
Time Frame
4 weeks
Title
Decrease in the duration of hospitalisation
Time Frame
4 weeks
Title
Adverse events of Dexamethasone and NAC in patients undergoing transarterial chemoembolisation for HCC
Time Frame
2 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients undergoing TACE procedure Valid Consent Age 18-65 years Exclusion Criteria: Child Pugh C, Child Pugh B > 8 HCC patients with a curative therapy (Ablation, Resection or LT) ECOG Performance Status 3-4 Pregnancy History of allergic reaction from NAC significant cardiopulmonary disease UGI bleed within last 28 days Recent surgery within last 28 days Documented febrile illness in last 1 weeks Uncontrolled Diabetes (FBS > 200, HBA1C > 8) Uncontrolled Hypertension (BP > 160/100) Structural kidney disease with eGFR < 60 ml/min
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dr Phool Chand, MD
Phone
01146300000
Email
phoolchand99@gmail.com
Facility Information:
Facility Name
Institute of Liver & Biliary Sciences
City
New Delhi
State/Province
Delhi
ZIP/Postal Code
110070
Country
India
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dr Phool Chand, MD
Phone
01146300000
Email
phoolchand99@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Comparison of Dexamethasone and N Acetylcysteine (NAC) Versus N Acetylcysteine (NAC) Alone in the Prevention of Post Embolization Syndrome in Patients With Hepatocellular Carcinoma Following Transarterial Chemoembolization.

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