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HBOT in the Treatment and Prevention of aGVHD

Primary Purpose

Hyperbaric Oxygen Therapy, Acute-graft-versus-host Disease

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Hyperbaric oxygen therapy
Sponsored by
Shandong Provincial Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hyperbaric Oxygen Therapy

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients undergoing allogeneic stem cell transplantation
  • Patients develop aGVHD
  • The count of neutrophilia cells over 0.5 * 109/L, hemoglobin over 60 g/L, platelet over 30 *109/L
  • Signed informed consent

Exclusion Criteria:

  • Unsuitable to the study due to severe complication such as uncontrolled severe infection
  • Claustrophobia
  • Ear diseases such as otitis media
  • Eye diseases such as glaucoma
  • Epilepsy history
  • Important organ dysfunction
  • Coagulopathy

Sites / Locations

  • Shandong Provincial HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

aGVHD-HBOT

aGVHD-HBOT free

Arm Description

Patients after allo-HSCT will receive hyperbaric oxygen therapy (HBOT) on the next day of the aGVHD diagnosis was determined.

Patients after allo-HSCT will NOT receive hyperbaric oxygen therapy (HBOT) on the next day of the aGVHD diagnosis was determined.

Outcomes

Primary Outcome Measures

Overall response rate of HBOT as complete response or partial response for the treatment of aGVHD
Complete or partial response rate of HBOT for the treatment of aGVHD will be measured using Bayesian method.
Incidence of aGVHD when HBOT was administrated as prophylaxis measurement at one month after transplant
At one month after transplant, HBOT will be administrated every three days (up to 6 times) to recipients without aGVHD evidence, the incidence of aGVHD will be counted.

Secondary Outcome Measures

Overall survival rate
Will be summarized by frequency and 95% confidence interval. The distribution of time-to-event endpoints will be estimated by Kaplan-Meier estimate. Comparison of time-to-event endpoints by important subgroups will be made using the log-rank test. Cox proportional hazards regression will be employed for multivariate analysis on time-to-event outcomes.
Leukemia-free survival rate
Will be summarized by frequency and 95% confidence interval. The distribution of time-to-event endpoints will be estimated by Kaplan-Meier estimate. Comparison of time-to-event endpoints by important subgroups will be made using the log-rank test. Cox proportional hazards regression will be employed for multivariate analysis on time-to-event outcomes.
Relapse rate
Relapse rate of recipients will be measured using Bayesian method. Will be summarized by frequency and 95% confidence interval.
Incidence of adverse events of HBOT
Toxicities will be summarized by grade and by their relationship to treatment.

Full Information

First Posted
September 6, 2021
Last Updated
October 13, 2021
Sponsor
Shandong Provincial Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05078073
Brief Title
HBOT in the Treatment and Prevention of aGVHD
Official Title
Hyperbaric Oxygen Therapy Improve Acute Graft-Versus-Host Disease in Patients Underwent Allogeneic Hematopoietic Stem Cell Transplantation
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Recruiting
Study Start Date
October 10, 2021 (Anticipated)
Primary Completion Date
August 10, 2024 (Anticipated)
Study Completion Date
August 10, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shandong Provincial Hospital

4. Oversight

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

5. Study Description

Brief Summary
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a potentially curative therapeutic strategy for patients with hematopoietic malignancies. However, the therapeutic benefits and wider application of allo-HSCT are limited by acute graft-versus-host disease (aGVHD), the latter remains a major obstacle against long-term survival for this population. New aGVHD prophylactic and therapeutic strategies that are superior in efficacy, safety, cost-effectiveness, and less technically demanding are still in desperate need. Hyperbaric oxygen therapy (HBOT) has been confirmed as an effective and economical therapeutic modality for hemorrhagic cystitis (HC) whether induced by infection or acute graft-versus-host disease (aGVHD) for transplant recipients. However, little is known about its involvement in aGVHD. In this study, the investigators designed a randomized, controlled, and open clinical trial to confirm the safety and efficacy of HBOT on aGVHD in patient underwent allo-HSCT.
Detailed Description
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a potentially curative therapeutic strategy for patients with hematopoietic malignancies. However, the therapeutic benefits and wider application of allo-HSCT are limited by acute graft-versus-host disease (aGVHD), the latter remains a major obstacle against long-term survival for this population. New aGVHD prophylactic and therapeutic strategies that are superior in efficacy, safety, cost-effectiveness, and less technically demanding are still in desperate need. Although a variety of immune and non-immune cells are involved in the development of aGVHD, reactive oxygen species (ROS) has been proved as the primary triggers of the inflammatory response and play a key role in the pathogenesis of aGVHD. Therefore, strategies targeting ROS production are crucial for effectively managing aGVHD. Hyperbaric oxygen therapy (HBOT) is a well-established treatment method, which is used to improve non-healing ulcers secondary to aGVHD and hemorrhagic cystitis (HC) after allo-HSCT whether induced by infection or aGVHD. Even the exact mechanism is not fully understood, HBOT was demonstrated to reduce a series of pro-inflammatory cytokines release and can improve the action of antibiotics. In this study, the investigators plan to initiate a randomized, controlled, and open clinical cohort study confirm the safety and efficacy of HBOT on aGVHD in patient underwent allo-HSCT.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hyperbaric Oxygen Therapy, Acute-graft-versus-host Disease

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
aGVHD-HBOT
Arm Type
Experimental
Arm Description
Patients after allo-HSCT will receive hyperbaric oxygen therapy (HBOT) on the next day of the aGVHD diagnosis was determined.
Arm Title
aGVHD-HBOT free
Arm Type
No Intervention
Arm Description
Patients after allo-HSCT will NOT receive hyperbaric oxygen therapy (HBOT) on the next day of the aGVHD diagnosis was determined.
Intervention Type
Device
Intervention Name(s)
Hyperbaric oxygen therapy
Intervention Description
Patients with aGVHD treated with HBOT every two days
Primary Outcome Measure Information:
Title
Overall response rate of HBOT as complete response or partial response for the treatment of aGVHD
Description
Complete or partial response rate of HBOT for the treatment of aGVHD will be measured using Bayesian method.
Time Frame
Four years
Title
Incidence of aGVHD when HBOT was administrated as prophylaxis measurement at one month after transplant
Description
At one month after transplant, HBOT will be administrated every three days (up to 6 times) to recipients without aGVHD evidence, the incidence of aGVHD will be counted.
Time Frame
100 days post transplant
Secondary Outcome Measure Information:
Title
Overall survival rate
Description
Will be summarized by frequency and 95% confidence interval. The distribution of time-to-event endpoints will be estimated by Kaplan-Meier estimate. Comparison of time-to-event endpoints by important subgroups will be made using the log-rank test. Cox proportional hazards regression will be employed for multivariate analysis on time-to-event outcomes.
Time Frame
Four years
Title
Leukemia-free survival rate
Description
Will be summarized by frequency and 95% confidence interval. The distribution of time-to-event endpoints will be estimated by Kaplan-Meier estimate. Comparison of time-to-event endpoints by important subgroups will be made using the log-rank test. Cox proportional hazards regression will be employed for multivariate analysis on time-to-event outcomes.
Time Frame
Four years
Title
Relapse rate
Description
Relapse rate of recipients will be measured using Bayesian method. Will be summarized by frequency and 95% confidence interval.
Time Frame
Four years
Title
Incidence of adverse events of HBOT
Description
Toxicities will be summarized by grade and by their relationship to treatment.
Time Frame
Four years

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients undergoing allogeneic stem cell transplantation Patients develop aGVHD The count of neutrophilia cells over 0.5 * 109/L, hemoglobin over 60 g/L, platelet over 30 *109/L Signed informed consent Exclusion Criteria: Unsuitable to the study due to severe complication such as uncontrolled severe infection Claustrophobia Ear diseases such as otitis media Eye diseases such as glaucoma Epilepsy history Important organ dysfunction Coagulopathy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yujie Jiang, Dr.
Phone
86-13370506886
Email
yujiejiang05@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xiaoming Zhou, Dr.
Organizational Affiliation
Shandong Provincial Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Shandong Provincial Hospital
City
Jinan
State/Province
Shandong
ZIP/Postal Code
250021
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaoming Zhou, Dr.

12. IPD Sharing Statement

Plan to Share IPD
No

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HBOT in the Treatment and Prevention of aGVHD

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