Carpal tunnel syndrome happens when pressure on the median nerve in the wrist causes numbness, tingling, and pain in the hand. It affects about 3% of adults in the US. Most people start with splinting and steroid injections, and many eventually have surgery to release pressure on the nerve.
What's actually going on in research
Trials are testing ultrasound-guided injections that may improve on standard steroid shots, nerve gliding exercises to reduce symptoms without surgery, and minimally invasive surgical techniques that reduce recovery time. Studies are also comparing different timing for surgery and looking at whether early treatment prevents permanent nerve damage.
Ultrasound-guided treatments
Injecting steroids under ultrasound guidance may target the compressed nerve more precisely than landmark-based injections. Some trials are testing whether this approach gives longer relief or helps more people avoid surgery.
Nerve and tendon gliding
Physical therapy protocols using specific hand and wrist exercises aim to reduce pressure on the median nerve. Studies are testing whether these exercises work as well as splinting for mild cases.
What to know before you search
Eligibility usually depends on symptom severity, nerve conduction test results, how long symptoms have lasted, and whether previous treatments have been tried.
What types of trials are currently open
- Injection trials — Comparing steroid injections to placebo or to each other, often testing ultrasound guidance or different injection techniques.
- Physical therapy trials — Testing exercise programs, splinting protocols, and manual therapy to see if they reduce symptoms without injections or surgery.
- Surgical technique trials — Comparing minimally invasive approaches to traditional open surgery, looking at recovery time, pain, and success rates.
- Prevention studies — Following people at risk for carpal tunnel to learn whether workplace changes, wrist exercises, or other interventions prevent the condition.
- Timing studies — Testing whether early surgery prevents nerve damage better than waiting to see if conservative treatment works.
Recently added Carpal Tunnel Syndrome trials
Receive an ultrasound-guided injection to treat carpal tunnel syndrome
Carpal tunnel syndrome (CTS) is a common peripheral nerve entrapment disorder caused by compression of the median nerve at the wrist. This study is a comparative study designed to evaluate the efficacy of three ultrasound-guided injection treatments for patients with mild to moderate CTS: hyaluronic acid (HA), corticosteroid, and 5% glucose (D5W). A total of 60 adult patients with clinically and electrophysiologically confirmed mild to moderate CTS will be enrolled and divided into three groups of 20 patients each. Participants will receive a single ultrasound-guided injection using one of the three study interventions. Clinical assessment will include Phalen's test and Tinel's sign. Electrophysiological assessment will include median nerve sensory and motor nerve conduction parameters, while ultrasonographic assessment will include measurement of the median nerve cross-sectional area. Participants will be reassessed three months after the intervention using the same clinical, electrophysiological, and ultrasonographic measures. The study will compare changes in these outcomes among the three treatment groups to evaluate their relative efficacy in the management of mild to moderate CTS.
Share outcomes from your carpal tunnel surgery experience
Carpal Tunnel Syndrome (CTS) is the most prevalent entrapment neuropathy. Open Surgical Carpal Tunnel Release (OSCTR) remains the gold standard, while minimally invasive Ultrasound-Guided Carpal Tunnel Release (USGCTR) offers potential advantages including reduced postoperative morbidity and faster recovery. This prospective, multicenter observational cohort study compares the clinical outcomes, patient-reported outcomes, and socioeconomic impact of USGCTR versus OSCTR. A total of 200 patients, with 100 patients per cohort, will be included. Patient assignment is based on the participating center's standard of care. Follow-up assessments are performed preoperatively and at 2 weeks, 6 weeks, 3 months, and 12 months after surgery.
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