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Comparison of the Effectiveness of Povidone-Iodine Alone to Povidone-Iodine-Tetracycline Combination

Primary Purpose

Malignant Pleural Effusion

Status
Unknown status
Phase
Phase 1
Locations
Nigeria
Study Type
Interventional
Intervention
CHEMICAL PLEURODESIS WITH POVIDONE-IODINE-TETRACYCLINE COMBINATION
CHEMICAL PLEURODESIS WITH POVIDONE-IODINE ALONE
Sponsored by
University College Hospital, Ibadan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malignant Pleural Effusion focused on measuring MALIGNANT PLEURAL EFFUSSION

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • • All adult patients aged between18- 70 years presenting with pleural effusion in association with a malignant disease.

    • Patients with documented malignant pleural effusion ( i.e positive pleural fluid for malignant cells on pleural fluid cytology and/or positive pleural biopsy for malignant tissue).
    • Reaccumulation of an effusion after drainage or patients presenting with symptoms related to pleural fluid re-accumulation such as dyspnea, cough and chest pain.
    • Patient with full lung re-expansion after thoracostomy tube insertion and drainage of effusion.

Exclusion Criteria:

  • • Patients with known hypersensitivity either to Povidone-iodine and/or Tetracycline

    • Failure to achieve full lung re-expansion following drainage of the effusion within 48hrs
    • Locoregional radiotherapy to the effusion side.
    • Loculated pleural effusion
    • Refusal to participate in the study

Sites / Locations

  • University College Hospital,Recruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

PATIENTS WITH MALIGNANT PLEURAL EFFUSION

PATEINT WITH MALIGANT PLEURAL EFFUSION REQUIRNG PLEURODESIS

Arm Description

PARTICIPANTS WITH MALIGNANT PLEURAL EFFUSIONS REQUIRING PLEURODESIS, COMBINATION OD POVIDONE IODOONE-TETRCYCLINE TO BE USED.

TO USE POVIDONE IODINE ALONE IN THIS GROUP

Outcomes

Primary Outcome Measures

Success of pleurodesis
classified as either a Complete Pleurodesis or Failed Pleurodesis. Complete pleurodesis defined as absence of pleural fluid re-accumulation on a chest radiograph at 1 and 3 months post-chemical pleurodesis, while Failed pleurodesis defined as pleural fluid re-accumulation requiring additional tube thoracostomy drainage before or at 1- 3 month follow up.

Secondary Outcome Measures

Adverse Effects from the chemical pleurodesis agent used
Adverse effects which are Post-procedure Pain, Hypotension, Fever and development of Empyema Thoracis following pleurodesis.

Full Information

First Posted
July 27, 2019
Last Updated
November 3, 2020
Sponsor
University College Hospital, Ibadan
Collaborators
West African College of Surgeons
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1. Study Identification

Unique Protocol Identification Number
NCT04039126
Brief Title
Comparison of the Effectiveness of Povidone-Iodine Alone to Povidone-Iodine-Tetracycline Combination
Official Title
Comparison of the Effectiveness of Povidone-Iodine Alone to Povidone-Iodine-Tetracycline Combination for Chemical Pleurodesis in Malignant Pleural Effusion
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
June 20, 2019 (Actual)
Primary Completion Date
December 2020 (Anticipated)
Study Completion Date
March 31, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University College Hospital, Ibadan
Collaborators
West African College of Surgeons

4. Oversight

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

5. Study Description

Brief Summary
Title of study: Comparison of the Effectiveness of Povidone-Iodine alone to Povidone-Iodine--Tetracycline Combination for Chemical Pleurodesis in Malignant Pleural Effusion. Research design: Prospective Randomized Controlled Clinical Trial. Background: Malignant pleural effusion (MPE) is commonly encountered in clinical practice among patients with malignancy. In addition to its association with major morbidities, it also poses a high risk of recurrence following drainage. Chemical pleurodesis is often required to achieve pleural adhesion and obliteration of the pleural space to prevent such recurrence. Several agents are in common use for chemical pleurodesis with mixed effectiveness.
Detailed Description
STRUCTURED SUMMARY Title of study: Comparison of the Effectiveness of Povidone-Iodine alone to Povidone-Iodine--Tetracycline Combination for Chemical Pleurodesis in Malignant Pleural Effusion. Research design: Prospective Randomized Controlled Clinical Trial. Background: Malignant pleural effusion (MPE) is commonly encountered in clinical practice among patients with malignancy. In addition to its association with major morbidities, it also poses a high risk of recurrence following drainage. Chemical pleurodesis is often required to achieve pleural adhesion and obliteration of the pleural space to prevent such recurrence. Several agents are in common use for chemical pleurodesis with mixed effectiveness. Methodology: 62 consenting but blinded patients with clinical features of MPE who are undergoing pleural drainage and have fulfilled the criteria for chemical pleurodesis will be grouped by block balanced randomization into two equal groups- A and B. All the patients in Group A (Test) will have pleurodesis done with a solution combining 1 gram of sterile Tetracycline powder with 20mls of 10% Povidone-iodinemixed with 10mls of 1% xylocaine (for local intrapleural anesthesia) and 30mls of sterile water for injection instilled through the chest tube into the pleural space, while allpatients in Group B (Active control) will have 20mls of 10% Povidone-iodine mixed with 10mls of 1% xylocaine and 30mls of sterile water for injection. Drainage and radiographic parameters will be collected prior to chest tube removal and during outpatient follow-up to assess the effectiveness of pleurodesis in each group. Objectives: To determine if combining tetracycline with 10% Povidone-iodine increases its effectiveness in pleurodesis for MPE. Principal Exposure:Chemical pleurodesis with 10% Povidone-Iodine or combination of 10% Povidone-iodine-Tetracycline (1 gram). Outcome variables: The primary outcome variable is the success of the pleurodesis in controlling MPE at 1month and 3 months follow-up. Success of pleurodesis classified as been Complete pleurosesis or Failed pleurodesis. The secondary outcome variables are: post-procedure complications of pain, hypotension,fever and occurrence of empyema thoracis, duration of thoracostomy tube retention post-pleurodesis, need for repeat of the procedure Keywords: Malignant Pleural Effusion, Chemical Pleurodesis, 10% Povidone-iodine, Tetracycline, Effectiveness

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malignant Pleural Effusion
Keywords
MALIGNANT PLEURAL EFFUSSION

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Masking Description
DOUBLE BLINDED, PARTIPANT ASIIGNED USING WINPEPI
Allocation
Randomized
Enrollment
62 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
PATIENTS WITH MALIGNANT PLEURAL EFFUSION
Arm Type
Experimental
Arm Description
PARTICIPANTS WITH MALIGNANT PLEURAL EFFUSIONS REQUIRING PLEURODESIS, COMBINATION OD POVIDONE IODOONE-TETRCYCLINE TO BE USED.
Arm Title
PATEINT WITH MALIGANT PLEURAL EFFUSION REQUIRNG PLEURODESIS
Arm Type
Active Comparator
Arm Description
TO USE POVIDONE IODINE ALONE IN THIS GROUP
Intervention Type
Drug
Intervention Name(s)
CHEMICAL PLEURODESIS WITH POVIDONE-IODINE-TETRACYCLINE COMBINATION
Other Intervention Name(s)
PLEURODESIS
Intervention Description
Pleurodesis is the obliteration of the pleural cavity by inducing adhesions of the visceral and parietal pleural layers, mostly used in patients with pleural effusions, pneumothorax (18). The use of pleurodesis to induce pleural symphysis between the pleural layers dates backs to the beginning of the 20th century by Benthune(19) and has continued to evolve with different Thoracic surgeons and researchers still looking for the ideal pleurodesis agent.
Intervention Type
Drug
Intervention Name(s)
CHEMICAL PLEURODESIS WITH POVIDONE-IODINE ALONE
Other Intervention Name(s)
PLEURODESE
Intervention Description
20mls of 10% povidone-iodine (Wosan Solution Povidone-Iodine Usp 10%, Jawa International Limited) is mixed with 10mls of 1% xylocaine and 30mls of water for injection added to the mixture, making also a total volume of 60mls of the the single pleurodesis agents alone, which will be instilled into the pleural space via the closed thoracotomy tube.
Primary Outcome Measure Information:
Title
Success of pleurodesis
Description
classified as either a Complete Pleurodesis or Failed Pleurodesis. Complete pleurodesis defined as absence of pleural fluid re-accumulation on a chest radiograph at 1 and 3 months post-chemical pleurodesis, while Failed pleurodesis defined as pleural fluid re-accumulation requiring additional tube thoracostomy drainage before or at 1- 3 month follow up.
Time Frame
1 AND 3 MONTH AFTER PLEURODESIS
Secondary Outcome Measure Information:
Title
Adverse Effects from the chemical pleurodesis agent used
Description
Adverse effects which are Post-procedure Pain, Hypotension, Fever and development of Empyema Thoracis following pleurodesis.
Time Frame
immediate post procedure( 30minutes and 1 hour)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: • All adult patients aged between18- 70 years presenting with pleural effusion in association with a malignant disease. Patients with documented malignant pleural effusion ( i.e positive pleural fluid for malignant cells on pleural fluid cytology and/or positive pleural biopsy for malignant tissue). Reaccumulation of an effusion after drainage or patients presenting with symptoms related to pleural fluid re-accumulation such as dyspnea, cough and chest pain. Patient with full lung re-expansion after thoracostomy tube insertion and drainage of effusion. Exclusion Criteria: • Patients with known hypersensitivity either to Povidone-iodine and/or Tetracycline Failure to achieve full lung re-expansion following drainage of the effusion within 48hrs Locoregional radiotherapy to the effusion side. Loculated pleural effusion Refusal to participate in the study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jibril Khalil, MMBS
Phone
+2348036602929
Email
jibril.khalil@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
MUDASSIRU SALAMI, MRCS
Phone
+2348023904206
Email
drmudathirsalami@yahoo.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
catherine Falade, Prof.
Organizational Affiliation
institute for advanced medical research and training, UI, IBADAN
Official's Role
Study Chair
Facility Information:
Facility Name
University College Hospital,
City
Ibadan
State/Province
Oyo
ZIP/Postal Code
200212
Country
Nigeria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jibril Khalil, MBBS
Phone
+2348036602929
Email
jibril.khalil@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
proforma of the study, with theinformation gathered during the study.
IPD Sharing Time Frame
as the study is being conducted
IPD Sharing Access Criteria
via email
Citations:
PubMed Identifier
27246596
Citation
Psallidas I, Kalomenidis I, Porcel JM, Robinson BW, Stathopoulos GT. Malignant pleural effusion: from bench to bedside. Eur Respir Rev. 2016 Jun;25(140):189-98. doi: 10.1183/16000617.0019-2016. Erratum In: Eur Respir Rev. 2016 Sep;25(141):360. Eur Respir Rev. 2016 Sep;25(141):360.
Results Reference
background
PubMed Identifier
11529302
Citation
Antony VB, Loddenkemper R, Astoul P, Boutin C, Goldstraw P, Hott J, Rodriguez Panadero F, Sahn SA. Management of malignant pleural effusions. Eur Respir J. 2001 Aug;18(2):402-19. doi: 10.1183/09031936.01.00225601. No abstract available.
Results Reference
background
PubMed Identifier
930945
Citation
Chernow B, Sahn SA. Carcinomatous involvement of the pleura: an analysis of 96 patients. Am J Med. 1977 Nov;63(5):695-702. doi: 10.1016/0002-9343(77)90154-1. No abstract available.
Results Reference
background

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Comparison of the Effectiveness of Povidone-Iodine Alone to Povidone-Iodine-Tetracycline Combination

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