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Hyperbaric Oxygen Therapy for Hemorrhagic Cystitis Post HSCT

Primary Purpose

Stem Cell Transplant Complications

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 Stem Cell Transplant Complications focused on measuring allogeneic stem cell transplantation, Hemorrhagic cystitis, Hyperbaric oxygen treatment

Eligibility Criteria

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

Inclusion Criteria:

  • Patients undergoing allogeneic stem cell transplantation
  • Patients develop late-onset hemorrhagic cystitis (HC)
  • The count of neutrophilia cells over 0.5 * 10^9/L, hemoglobin over 60 g/L, platelet over 30 *10^9/L
  • SGOT/SGPT no more than 2 times of UNL
  • Serum creatinine no more than 1.5 times of UNL
  • Signed informed consent

Exclusion Criteria:

  • Early-onset HC post-allo-HSCT
  • 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 Type

Experimental

Arm Label

HBOT group

Arm Description

Patients with hemorrhagic cystitis (HC) after allo-HSCT will receive hyperbaric oxygen therapy (HBOT) on the next day of the HC diagnosis was determined. Then HBOT will be scheduled every day until symptoms of HC vanished.

Outcomes

Primary Outcome Measures

Response rate of HBOT
Response rate of HBOT was determined on the basis of HC symptom disppearance and the normal urine routine test result
Incidence and severity of treatment-related adverse events
Number of participants with treatment-related adverse events and the the severity of these events.

Secondary Outcome Measures

Exploratory biomarker analysis
Exploratory biomarker to predict treatment response

Full Information

First Posted
July 30, 2020
Last Updated
September 6, 2021
Sponsor
Shandong Provincial Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04502628
Brief Title
Hyperbaric Oxygen Therapy for Hemorrhagic Cystitis Post HSCT
Official Title
Hyperbaric Oxygen Therapy for the Treatment of Hemorrhagic Cystitis Post Allogeneic Hematopoietic Stem Cell Transplantation
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2021 (Anticipated)
Primary Completion Date
July 31, 2023 (Anticipated)
Study Completion Date
December 31, 2024 (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
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a potentially curative therapy for many malignant or nonmalignant hematological diseases. Hemorrhagic cystitis (HC) is one of the common and major causes of morbidity in patients undergoing allo-HSCT. Its incidence ranges from 7 to 52%, and its manifestations range from painless microscopic hematuria to severe bladder hemorrhage, leading to clot formation within the urinary tract and even renal failure. This complication results in much pain to the patient and increasing treatment cost. Late-onset HC (two weeks after stem cell infusion) has been associated with reactivation of viruses, including cytomegalovirus, polyoma BK and JC viruses, and adenovirus types I and II. Former studies have confirmed that the bladder is also considered to be one of the immune attacked organs in acute graft-versus-host disease (aGVHD). The classic treatments for HC include hydration, alkalization, and bladder irrigation, immunosuppressant reduction, and platelet transfusion. Patients with viral infection may be treated with antiviral agents, but their efficacy is limited. When the HC was considered to be associated with aGVHD, some immunosuppressive agents such as glucocorticoids will be added in. However, too intensive immunosuppressive measures leave the patients susceptible to infection and, in turn, increases the accidence of non-relapse mortality (NRM). The mechanism underlying the development of HC remains largely unidentified, and its optimal treatment has not yet been established. It is important to explore novel, less-toxic, higher effective, and cost-effective strategies to improve HC. The elevated levels of available oxygen and partial pressure of arterial oxygen provide the main benefits of Hyperbaric oxygen therapy (HBOT) in clinical practice that addresses these areas of inadequate or poor tissue healing. HBOT is utilized as primary or adjunctive therapy for many medical conditions in which tissue damage is triggered by hypoxic injury. The pharmacological and physiologic effects of HBOT have direct and indirect mechanisms and effects on reactive oxygen species (ROS) most beneficial to that of wound healing and antibacterial treatments. HBOT can stimulate fibroblast proliferation, angiogenesis, and wound healing. It has been shown effective in the treatment of radiation-induced HC by promoting fibroblast proliferation and capillary angiogenesis, decreasing edema, and facilitating damaged hypoxic urothelium. Based on the above clinical and pre-clinical practice, the investigators deduce that HBOT may benefit patients with HC after HSCT. In the investigators' limited early-onset investigation, the investigators found HBO was largely successful in 20 patients suffering HC post-allo-HSCT, showed a quick resolution or improvement of HC. The investigators also observed more rapid responses in patients who started HBOT earlier after the diagnosis of HC. The investigators confirmed that HBOT was effective and well-tolerated in the patients, regardless of the infective- or non-infective- caused HC. Therefore, the investigators design this prospective, randomized, and single-arm clinical trial to establish the definitive efficacy and safety of HBOT in patients with HC after allo-HSCT.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stem Cell Transplant Complications
Keywords
allogeneic stem cell transplantation, Hemorrhagic cystitis, Hyperbaric oxygen treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
HBOT group
Arm Type
Experimental
Arm Description
Patients with hemorrhagic cystitis (HC) after allo-HSCT will receive hyperbaric oxygen therapy (HBOT) on the next day of the HC diagnosis was determined. Then HBOT will be scheduled every day until symptoms of HC vanished.
Intervention Type
Procedure
Intervention Name(s)
Hyperbaric oxygen therapy
Intervention Description
Patients with hemorrhagic cystitis (HC) after allo-HSCT will receive hyperbaric oxygen therapy (HBOT) on the next day of the HC diagnosis was determined. Then HBOT will be scheduled every day until symptoms of HC vanished. Other classic measures to treatment HC such as hydration, alkalization, and bladder irrigation will also be carried out at the same time.
Primary Outcome Measure Information:
Title
Response rate of HBOT
Description
Response rate of HBOT was determined on the basis of HC symptom disppearance and the normal urine routine test result
Time Frame
Six months post-allo-HSCT
Title
Incidence and severity of treatment-related adverse events
Description
Number of participants with treatment-related adverse events and the the severity of these events.
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Exploratory biomarker analysis
Description
Exploratory biomarker to predict treatment response
Time Frame
3 years

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients undergoing allogeneic stem cell transplantation Patients develop late-onset hemorrhagic cystitis (HC) The count of neutrophilia cells over 0.5 * 10^9/L, hemoglobin over 60 g/L, platelet over 30 *10^9/L SGOT/SGPT no more than 2 times of UNL Serum creatinine no more than 1.5 times of UNL Signed informed consent Exclusion Criteria: Early-onset HC post-allo-HSCT 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 M JIANG
Phone
8613370506886
Ext
8613370506886
Email
yujiejiang05@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xin Wang
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
Yujie JIANG
Phone
8613370506886
Email
yujiejiang05@126.com

12. IPD Sharing Statement

Plan to Share IPD
No

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Hyperbaric Oxygen Therapy for Hemorrhagic Cystitis Post HSCT

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