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Efficacy of hyperbaric oxygen combined with functional operation therapy in patients with cervical cord injury

Efficacy of hyperbaric oxygen combined with functional operation therapy in patients with cervical cord injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102883
Enrollment
Unknown
Registered
2025-05-21
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical spinal cord injury

Interventions

combined treatment group:The combined group was given hyperbaric oxygen therapy combined with functional occupational therapy on the basis of conventional rehabilitation treat.
Hyperbaric oxygen therapy group:Patients in the hyperbaric oxygen group received hyperbaric oxygen therapy on the basis of conventional rehabilitation treatment.
Functional occupational therapy group:Patients in the functional occupational therapy group were given functional occupational therapy training on the basis of conventional rehabilitation .

Sponsors

Beijing Bo'ai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Imaging examination shows that the patient meets the diagnostic criteria of SCI; (2) Traumatic cervical spinal cord injury with C and D grades conforming to the international standard diagnosis of spinal cord injury neurological classification, and the injured segment is C5~C7; (3) Age between 18 and 65; (4) The course of injury is within 6 months; (5) The modified Ashworth scale was graded less than grade II; (6) The patient or his/her family members agree to participate in the trial and sign an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients with combined limb fractures or severe skin injuries that affect rehabilitation training; (2) Patients with deep vein thrombosis, blood coagulation disorders, malignant tumors and infectious diseases; (3) Severe dysfunction or chronic diseases of important organs such as heart, brain, liver, kidney and lung; (4) Epilepsy or mental illness; (5) Patients with contraindications to hyperbaric oxygen therapy and unable to undergo hyperbaric oxygen therapy.

Design outcomes

Primary

MeasureTime frame
Assessment of daily living activities;Upper limb motor function assessment;

Secondary

MeasureTime frame
Joint mobility assessment;Quality of life measurement;Emotional assessment;Upper limb circumference;cognitive function;Upper limb function questionnaire;Near infrared testing;Muscle tone assessment;Serum factor assessment;sensory function;Vascular endothelial growth factor ;Inducible nitric oxide synthase;Brain-derived neurotrophic factor ;

Countries

China

Contacts

Public ContactLi Xiuli

Beijing Bo'ai Hospital

13811718745@163.com+86 138 1171 8745

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026