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Study to Determine if Hyperbaric Oxygen Therapy is Helpful for Treating Radiation Tissue Injuries

Primary Purpose

Radiation Injuries

Status
Terminated
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Hyperbaric Oxygen Therapy
Sham treatment
Sponsored by
National Baromedical Services
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Radiation Injuries focused on measuring Hyperbaric Oxygenation, Radiation injuries, Prophylaxis, Proctitis, Cystitis, Enteritis, Osteoradionecrosis

Eligibility Criteria

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

Inclusion Criteria: Endarteritis Hypovascularity Diarrhea Cramping Obstruction Stricture Pain Hemorrhage Wall Changes Ulceration Hypocellularity Mucosal thickening Vomiting Tenesmus Constipation Perforation Fistula Obstipation Tissue hypoxia Exclusion Criteria: Pregnancy Reactive airway disease Radiographic evidence of pulmonary blebs or bullae Untreated pneumothorax Previously documented ejection fraction less than 35% History of seizures except childhood febrile seizures Cardiovascular instability Mechanical ventilator support with the exception of those patients who are immediately (1-5 days) post-operative Unable to follow simple commands Not orientated to person, place, time Participating as a subject in any other medical or biomedical research project; if previously involved as a subject, sufficient time must have elapsed to permit "wash out" of any investigational agent.

Sites / Locations

  • Palmetto Health Richland
  • Wesley Medical Center
  • Royal Hobart Hospital
  • Instituto Nacional de Cancerologica
  • University of Stellenbosch
  • University of Pretoria Medical Center
  • Istanbul University Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

A

B

Arm Description

Hyperbaric Oxygen Therapy

Normal Air

Outcomes

Primary Outcome Measures

SOMA (Subjective, Objective, Management, Analytic) scale used to determine late effects to normal tissue (LENT) score

Secondary Outcome Measures

Clinical assessment using one of the following criteria:
Healed
Modestly improved (< 50% lesion resolution)
Not improved
Other (e.g. lesion recurrence, lesion size progression)
Significant Improvement (>50% lesion resolution)

Full Information

First Posted
August 23, 2005
Last Updated
January 11, 2016
Sponsor
National Baromedical Services
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1. Study Identification

Unique Protocol Identification Number
NCT00134628
Brief Title
Study to Determine if Hyperbaric Oxygen Therapy is Helpful for Treating Radiation Tissue Injuries
Official Title
Hyperbaric Oxygen Radiation Tissue Injury Study - Project HORTIS
Study Type
Interventional

2. Study Status

Record Verification Date
February 2012
Overall Recruitment Status
Terminated
Why Stopped
Discontinued cystitis study due to poor recruitment. To continue the trial under these circumstances is considered non-viable.
Study Start Date
January 2001 (undefined)
Primary Completion Date
August 2011 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National Baromedical Services

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The principle objective of this research is to more precisely determine the degree of benefit that hyperbaric oxygen therapy affords in the treatment of late radiation tissue injury. The study has eight* components. Seven involve the evaluation of established radionecrosis at varying anatomic sites (mandible, larynx, skin, bladder, rectum, colon, and gyn). The eighth will investigate the potential of hyperbaric oxygen (HBO) therapy to prophylax against late radiation tissue injury. *(One of the arms, HORTIS IV - Proctitis has been closed to further patient recruitment. This decision was based on an interim statistical analysis which generated sufficient evidence to support closing down this arm of HORTIS.)
Detailed Description
Radiation therapy is a key component of the control and eradication of malignant disease. Adequate tumoricidal doses may, however, result in damage to surrounding healthy tissue. Therapeutic radiation injuries to non-target tissues can be divided into acute, sub-acute, and delayed complications. Acute injuries are considered a direct cellular toxicity, self-limiting, and in most cases successfully managed symptomatically. Sub-acute injuries are typically identifiable in only a few organ systems, e.g., radiation pneumonitis. These, too, are generally limited but occasionally evolve to late complications. Late changes occur several months to many years after completing radiotherapy. The etiology of radiation's late effects to normal tissue (LENT) varies somewhat between organ systems. Its hallmark, however, is one of culminating in an obliterative endarteritis, and local hypoxia. The incidence of LENT is related to both total radiation exposure and the length of time a patient is out from completing radiotherapy. The higher the dose, the longer the interval from exposure, the greater the risk. In many cases, resulting radionecrotic lesions seriously impair form and function, and require extensive surgical correction or repair. Such surgery is fraught with complications, hence the inclusion of a "prophylactic" hyperbaric oxygen arm. A disturbing degree of mortality further complicates the development of LENT. Hyperbaric oxygen has been utilized in the treatment of radiation tissue injury for several decades. Most of the supportive basic science and clinical evidence stems from the management of mandibular osteoradionecrosis. More recently, the use of hyperbaric oxygen has been extended to other anatomic sites. This expanded use is based, in large part, on a presumed common underlying pathophysiology of LENT, regardless of its anatomic location. Supportive clinical evidence for these other sites is limited, however, and in need of a greater degree of scientific scrutiny.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Radiation Injuries
Keywords
Hyperbaric Oxygenation, Radiation injuries, Prophylaxis, Proctitis, Cystitis, Enteritis, Osteoradionecrosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Crossover Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
248 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Active Comparator
Arm Description
Hyperbaric Oxygen Therapy
Arm Title
B
Arm Type
Sham Comparator
Arm Description
Normal Air
Intervention Type
Procedure
Intervention Name(s)
Hyperbaric Oxygen Therapy
Intervention Description
HBO at 2.0 ATA
Intervention Type
Procedure
Intervention Name(s)
Sham treatment
Intervention Description
Normal air under pressure (1.1 ATA)
Primary Outcome Measure Information:
Title
SOMA (Subjective, Objective, Management, Analytic) scale used to determine late effects to normal tissue (LENT) score
Time Frame
pre-treatment, post-treatment (HBO and placebo) and at follow ups at 3 months, 6 months, and 1 year through 5 years
Secondary Outcome Measure Information:
Title
Clinical assessment using one of the following criteria:
Time Frame
post-treatment (HBO and placebo) and at follow ups at 3 months, 6 months, and 1 year through 5 years
Title
Healed
Time Frame
post-treatment (HBO and placebo) and at follow ups at 3 months, 6 months, and 1 year through 5 years
Title
Modestly improved (< 50% lesion resolution)
Time Frame
post-treatment (HBO and placebo) and at follow ups at 3 months, 6 months, and 1 year through 5 years
Title
Not improved
Time Frame
post-treatment (HBO and placebo) and at follow ups at 3 months, 6 months, and 1 year through 5 years
Title
Other (e.g. lesion recurrence, lesion size progression)
Time Frame
post-treatment (HBO and placebo) and at follow ups at 3 months, 6 months, and 1 year through 5 years
Title
Significant Improvement (>50% lesion resolution)
Time Frame
post-treatment (HBO and placebo) and at follow ups at 3 months, 6 months, and 1 year through 5 years

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Endarteritis Hypovascularity Diarrhea Cramping Obstruction Stricture Pain Hemorrhage Wall Changes Ulceration Hypocellularity Mucosal thickening Vomiting Tenesmus Constipation Perforation Fistula Obstipation Tissue hypoxia Exclusion Criteria: Pregnancy Reactive airway disease Radiographic evidence of pulmonary blebs or bullae Untreated pneumothorax Previously documented ejection fraction less than 35% History of seizures except childhood febrile seizures Cardiovascular instability Mechanical ventilator support with the exception of those patients who are immediately (1-5 days) post-operative Unable to follow simple commands Not orientated to person, place, time Participating as a subject in any other medical or biomedical research project; if previously involved as a subject, sufficient time must have elapsed to permit "wash out" of any investigational agent.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dick Clarke, CHT
Organizational Affiliation
National Baromedical Services
Official's Role
Principal Investigator
Facility Information:
Facility Name
Palmetto Health Richland
City
Columbia
State/Province
South Carolina
ZIP/Postal Code
29203
Country
United States
Facility Name
Wesley Medical Center
City
Brisbane
State/Province
Queensland
ZIP/Postal Code
4064
Country
Australia
Facility Name
Royal Hobart Hospital
City
Hobart
State/Province
Tasmania
ZIP/Postal Code
7001
Country
Australia
Facility Name
Instituto Nacional de Cancerologica
City
Mexico City
ZIP/Postal Code
14080
Country
Mexico
Facility Name
University of Stellenbosch
City
Cape Town
Country
South Africa
Facility Name
University of Pretoria Medical Center
City
Pretoria
ZIP/Postal Code
0001
Country
South Africa
Facility Name
Istanbul University Medical Center
City
Istanbul
ZIP/Postal Code
34390
Country
Turkey

12. IPD Sharing Statement

Citations:
PubMed Identifier
9191633
Citation
Curi MM, Dib LL. Osteoradionecrosis of the jaws: a retrospective study of the background factors and treatment in 104 cases. J Oral Maxillofac Surg. 1997 Jun;55(6):540-4; discussion 545-6. doi: 10.1016/s0278-2391(97)90478-x.
Results Reference
background
PubMed Identifier
4703530
Citation
Joseph DL, Shumrick DL. Risks of head and neck surgery in previously irradiated patients. Arch Otolaryngol. 1973 May;97(5):381-4. doi: 10.1001/archotol.1973.00780010393005. No abstract available.
Results Reference
background
PubMed Identifier
8285524
Citation
Samuels L, Granick MS, Ramasastry S, Solomon MP, Hurwitz D. Reconstruction of radiation-induced chest wall lesions. Ann Plast Surg. 1993 Nov;31(5):399-405. doi: 10.1097/00000637-199311000-00003.
Results Reference
background
PubMed Identifier
949677
Citation
Hart GB, Mainous EG. The treatment of radiation necrosis with hyperbaric oxygen (OHP). Cancer. 1976 Jun;37(6):2580-5. doi: 10.1002/1097-0142(197606)37:63.0.co;2-h.
Results Reference
background
PubMed Identifier
6572704
Citation
Marx RE. Osteoradionecrosis: a new concept of its pathophysiology. J Oral Maxillofac Surg. 1983 May;41(5):283-8. doi: 10.1016/0278-2391(83)90294-x.
Results Reference
background
PubMed Identifier
6574217
Citation
Marx RE. A new concept in the treatment of osteoradionecrosis. J Oral Maxillofac Surg. 1983 Jun;41(6):351-7. doi: 10.1016/s0278-2391(83)80005-6. No abstract available.
Results Reference
background
PubMed Identifier
7674746
Citation
Bevers RF, Bakker DJ, Kurth KH. Hyperbaric oxygen treatment for haemorrhagic radiation cystitis. Lancet. 1995 Sep 23;346(8978):803-5. doi: 10.1016/s0140-6736(95)91620-2.
Results Reference
background
PubMed Identifier
9231688
Citation
Woo TC, Joseph D, Oxer H. Hyperbaric oxygen treatment for radiation proctitis. Int J Radiat Oncol Biol Phys. 1997 Jun 1;38(3):619-22. doi: 10.1016/s0360-3016(97)00017-5.
Results Reference
background
PubMed Identifier
1497044
Citation
Williams JA Jr, Clarke D, Dennis WA, Dennis EJ 3rd, Smith ST. The treatment of pelvic soft tissue radiation necrosis with hyperbaric oxygen. Am J Obstet Gynecol. 1992 Aug;167(2):412-5; discussion 415-6. doi: 10.1016/s0002-9378(11)91421-5.
Results Reference
background
PubMed Identifier
8286987
Citation
Feldmeier JJ, Heimbach RD, Davolt DA, Brakora MJ. Hyperbaric oxygen as an adjunctive treatment for severe laryngeal necrosis: a report of nine consecutive cases. Undersea Hyperb Med. 1993 Dec;20(4):329-35.
Results Reference
background

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Study to Determine if Hyperbaric Oxygen Therapy is Helpful for Treating Radiation Tissue Injuries

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