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Enrolling by Invitation

NCT Number: NCT07191808

EXPLORING EFFECTIVENESS OF LOW LEVEL LASER THERAPY IN THE TREATMENT OF PATIENTS WITH BELLS PALSY

The aim of the proposed research is to explore effectiveness of Low Level LASER Therapy in the country and to compare its effectiveness with routine physiotherapy. The societal benefit of submitted research is to formulate a guideline for physical therapy clinicians of the country to treat patients with Bell's Palsy through modern tool of Low Level LASER Therapy if found effective for improvement in quality of lives

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

NACE

Faisalābad, 38090, Pakistan

About this study

Annually, incidence of Bell's Palsy ranges between 1 to 4 per 10,000 individuals globally. From Pakistan figures highlight that the incidence rate of Bell's palsy in Pakistan may be above the international average, with many patients reporting a decline in their quality-of-life post diagnosis.

Low-Level Laser Therapy (LLLT), a modality known as photobiomodulation, has woven its way through various medical settings over the past decades. It has found applications in promoting wound healing, alleviating musculoskeletal pain, and now is being explored in the realm of neurological recovery. This non-invasive therapeutic technique employs non-thermal lasers or LEDs, aiming to stimulate and enhance the functions of our cellular machinery.

Globally Studies have proved effectiveness of Low Level LASER therapy in Bell's Palsy, with reduction of recovery time, improvement of Quality of Life and Personal wellbeing of patients of Bell's Palsy. We performed a survey exploring treatment preferences of Physical Therapy Clinicians to treat patients with Bell's Palsy; result showed routine contemporary practices of physiotherapy with Low Level LASER Therapy were low as 8% professionals.

The target population in this study will be assessed with standard outcome measures including FDI, HBS, FNLT / NCS and SBFGS. Two outcome measures FDI and HBS has been translated in Urdu and Reliability Studies have also been completed with permission from the Authors. A Case Control study has also been completed considering the risk factors for patients with Bell's Palsy. A Systematic Review completed by the researcher also found the Gap to explore the effectiveness of Low Level LASER Therapy for patients with Bell's Palsy.

The aim of the proposed research is to explore effectiveness of Low Level LASER Therapy in the country and to compare its effectiveness with routine physiotherapy. The societal benefit of submitted research is to formulate a guideline for physical therapy clinicians of the country to treat patients with Bell's Palsy through modern tool of Low Level LASER Therapy if found effective for improvement in quality of lives.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • • A confirmed diagnosis of idiopathic facial (Bell's) palsy by a certified neurologist or Physician is required (Heckmann, Urban, Pitz, Guntinas-Lichius, & Gágyor, 2019).
  • Both male and female patients, aged between 18 and 80 years (Holland & Bernstein, 2014).
  • Symptom onset within the range of 72 hours to 7 days (Petruzzelli & Hirsch, 1991).
  • A baseline House-Brackmann score of 2 to 4 is necessary (Bylund et al., 2021).
  • Availability for the entire trial duration and all subsequent follow-up visits.
  • Absence of any prior treatments (e.g., corticosteroids) for the current Bell's palsy episode.

Exclusion criteria

  • • Alternate diagnoses that can explain Bell's palsy (e.g., Lyme disease, Ramsay Hunt syndrome) (Crouch, Hohman, Moody, & Andaloro, 2023).
  • History of recurrent Bell's palsy episodes.
  • Presence of severe medical conditions such as uncontrolled diabetes or autoimmune disorders.
  • Pregnancy or lactation. Use of concurrent medications that could interfere with facial nerve function.
  • Exposure to LLLT in the past 3 months.
  • Active skin infections or lesions in the targeted treatment area.
  • Conditions or medications that induce photosensitivity.
  • Cognitive impairments that may interfere with comprehension or feedback about the trial.
  • Participation in another trial in the past month.
  • Traumatic, inflammatory, or infectious conditions including trauma, nerve root issues, metabolic/spinal pathologies, previous spinal surgeries, or postpartum pain due to pregnancy (Singh & Deshmukh, 2022)

Treatment and study plan

Low Level Laser Therapy

Other

cluster method

Primary outcomes

  1. House-Brackmann Score

    Time frame: 6 weeks

    This scale is recognized for its capability to grade facial nerve dysfunction levels. The primary indicator of the treatment's efficacy will be any discernible improvement or non-worsening on this scale

Sponsors and collaborators

Lead sponsor

University of Lahore

Other

Registry information

Acronym: bells palsy

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Sep 25, 2025
Registry last updated
Sep 25, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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