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SciaticaNCT07710924

Effects of Shockwave Therapy Versus Ultrasound Therapy Among Patients With Chronic Sciatica

A study testing Extracorporeal Shockwave Therapy, Therapeutic Ultrasound and Conventional Physiotherapy in people with Sciatica and Chronic Sciatica, run by University of Lahore at 1 site in Pakistan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Sciatica is characterized by radiating pain, functional limitations, reduced flexibility, disturbed sleep, and impaired quality of life. Extracorporeal Shockwave Therapy (ESWT) and Therapeutic Ultrasound are commonly used physiotherapy modalities for pain relief and tissue healing; however, evidence directly comparing… Read more about this study

Who is it for?
Ages 20 to 45 years
Conditions the study is for
Sciatica, Chronic Sciatica, Lumbar Radiculopathy
What is being tested?
Extracorporeal Shockwave Therapy, Therapeutic Ultrasound and Conventional Physiotherapy
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
66 participants
Where
1 sitePakistan
Study dates
30 Jun 2025to 12 Apr 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 45 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Adults aged 20-45 years.
  • Clinically diagnosed chronic sciatica.
  • Radiating pain below the knee.
  • Positive Straight Leg Raise test (30°-70°).
  • Pain intensity ≥4/10 on the Numeric Pain Rating Scale.
  • Symptoms persisting for at least 3 months.
  • Presence of tingling, numbness, lumbar radiculopathy, or piriformis syndrome.

Who cannot join

  • Lumbar disc herniation.
  • Progressive neurological disorders.
  • Ankylosing spondylitis.
  • Paget disease.
  • Tuberculosis.
  • Malignancy.
Show all 9Show fewer
  • Rheumatoid arthritis or other inflammatory disorders.
  • Previous spinal surgery or fracture.
  • Fever, unexplained weight loss, or systemic illness.

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • ULTH

    Lahore

Other trials in Pakistan

About this study

Official title: Comparative Effects of Shockwave Therapy Versus Ultrasound Therapy Combined With Conventional Physiotherapy on Pain Intensity, Hamstring Range of Motion, Sleep Quality, and Quality of Life Among Patients With Chronic Sciatica: A Randomized Controlled Trial

Sciatica is characterized by radiating pain, functional limitations, reduced flexibility, disturbed sleep, and impaired quality of life. Extracorporeal Shockwave Therapy (ESWT) and Therapeutic Ultrasound are commonly used physiotherapy modalities for pain relief and tissue healing; however, evidence directly comparing their effectiveness remains limited. This randomized controlled trial compares the effects of Shockwave Therapy and Ultrasound Therapy, each combined with conventional physiotherapy, on pain intensity, hamstring range of motion, sleep quality, and quality of life in patients with chronic sciatica.

Read the detailed description

This randomized controlled trial compares two physiotherapy interventions for chronic sciatica. Sixty-six participants will be randomly allocated to either Shockwave Therapy plus Conventional Physiotherapy or Ultrasound Therapy plus Conventional Physiotherapy. Both groups will receive identical conventional physiotherapy consisting of heat therapy, myofascial release, stretching, and strengthening exercises. Treatment will be administered four sessions per week for eight weeks. Outcomes including pain intensity, hamstring range of motion, sleep quality, and quality of life will be measured at baseline, Week 4, and Week 8 by a blinded outcome assessor.

Being tested
Extracorporeal Shockwave Therapy, Therapeutic Ultrasound, Conventional Physiotherapy
Keywords
Sciatica, Chronic Sciatica, Lumbar Radiculopathy, Shockwave Therapy, Extracorporeal Shockwave Therapy
Medical subject headings
Sciatica, Radiculopathy

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Extracorporeal Shockwave TherapyDevice

    Also called ESWT, Radial Shockwave Therapy

    Radial extracorporeal shockwave therapy will be applied to the sciatic nerve origin and piriformis region using standardized treatment parameters for approximately 10 minutes during each treatment session.

  • Therapeutic UltrasoundDevice

    Also called Ultrasound Therapy, Ultrasound

    Therapeutic ultrasound will be applied to the gluteal and lumbar regions using standardized frequency and intensity parameters for approximately 10 minutes during each treatment session.

  • Conventional PhysiotherapyOther

    Conventional physiotherapy will include moist heat therapy, myofascial release, stretching exercises, and strengthening exercises administered during every treatment session.

Study groups in NCT07710924
Study groupRoleWhat they receive
Shockwave Therapy + Conventional PhysiotherapyExperimentalParticipants will receive radial extracorporeal shockwave therapy in addition to standardized conventional physiotherapy four times per week for eight weeks.
Receives: Device: Extracorporeal Shockwave Therapy; Other: Conventional Physiotherapy
Ultrasound Therapy + Conventional PhysiotherapyActive comparatorParticipants will receive therapeutic ultrasound in addition to standardized conventional physiotherapy four times per week for eight weeks.
Receives: Device: Therapeutic Ultrasound; Other: Conventional Physiotherapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pain Intensity

    Numeric Pain Rating Scale (0-10). Higher scores indicate greater pain.

    Measured: Baseline, Week 4, Week 8

  2. Hamstring Range of Motion

    Hip flexion measured with a universal goniometer during the Straight Leg Raise test.

    Measured: Baseline, Week 4, Week 8

Secondary outcomes (1)
  1. Sleep Quality

    Sleep Quality Scale. Higher scores indicate poorer sleep quality.

    Measured: Baseline, Week 4, Week 8

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Jul 2026
  2. Study start30 Jun 2025
  3. Primary completion10 Mar 2026
  4. Study completion12 Apr 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Participants will be randomly assigned in a 1:1 ratio to receive either Shockwave Therapy plus Conventional Physiotherapy or Ultrasound Therapy plus Conventional Physiotherapy. Both groups will receive the same conventional physiotherapy program, while the experimental intervention will differ according to treatment allocation. Outcome assessments will be conducted at baseline, Week 4, and Week 8 by a blinded assessor.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
66 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07710924
Sponsor's protocol ID
UOL/IREB/25/09/0054
Status last verified
Jul 2026
First submitted
14 Jul 2026
Last updated
17 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual participant data will not be shared because this study was conducted as an academic research project. The informed consent obtained from participants did not include provisions for public data sharing, and the dataset contains sensitive personal health information. Data will be stored securely and used only for academic and research purposes in accordance with institutional ethics approval.

Questions about this trial

What is this clinical trial studying?

A study testing Extracorporeal Shockwave Therapy, Therapeutic Ultrasound and Conventional Physiotherapy in people with Sciatica and Chronic Sciatica, run by University of Lahore at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 17 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Pain Intensity (time frame: Baseline, Week 4, Week 8). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Jul 2026.

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