To study the effect of HBOT in patients with Bells Palsy

To study the effects of HBOT in patients with Bells Palsy - NIL

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/08/072164

Enrollment

Registered

2024-08-08

Start date

Unknown

Completion date

Unknown

Last updated

2024-08-19

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

Conditions

Health Condition 1: G510- Bells palsy

Interventions

Intervention1: Medical Oxygen: Medical Oxygen given at fixed intervals in hyperbaric chamber as already being done in Hyperbaric Oxygen Treatment. Control Intervention1: Normal Air: Patients who are n

Eligibility

Inclusion criteria

Inclusion criteria: Patients with a House Brackman Grade of 3 and above will only be considered for HBOT.

Exclusion criteria

Exclusion criteria: Patients must not have any active lung disease or any other contraindication for HBOT.

Design outcomes

Primary

Measure	Time frame
To study the symptomatic improvement of lagophthalmos in patients of Bell’s Palsy undergoing HBOTTimepoint: 10 days, 20 days	—

Secondary

Measure	Time frame
NILTimepoint: NIL	—

Countries

India

Contacts

Public ContactC S Mohanty

INHS Asvini

drmohantycs@gmail.com400005

Outcome results

None listed

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