# Comparison of Progel Sealant to Standard of Care (SOC) for Patients Undergoing Decortication

> **NCT02511600** · PHASE3 · WITHDRAWN · sponsor: **M.D. Anderson Cancer Center**

## Conditions studied

- Lung Diseases
- Mesothelioma

## Interventions

- **OTHER:** Progel Sealant
- **OTHER:** Talcum Powder
- **BEHAVIORAL:** Pain Questionnaire

## Key facts

- **NCT ID:** NCT02511600
- **Lead sponsor:** M.D. Anderson Cancer Center
- **Sponsor class:** OTHER
- **Phase:** PHASE3
- **Study type:** INTERVENTIONAL
- **Status:** WITHDRAWN
- **Start date:** 2015-12
- **Primary completion:** 2018-12
- **Final completion:** —
- **Target enrollment:** 0 (ACTUAL)
- **Last updated:** 2015-12-15

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02511600

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02511600, "Comparison of Progel Sealant to Standard of Care (SOC) for Patients Undergoing Decortication". Retrieved via AI Analytics 2026-06-14 from https://api.ai-analytics.org/clinical/NCT02511600. Licensed CC0.

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