Muscle Pain

3

Review clinical trials related to Muscle Pain. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Jaw Muscle Pain Post Wisdom Molar Surgery

The proposed design is a triple-blind, placebo-controlled randomized prospective phase II trial to assess the feasibility of employing the Temporo-masseteric Nerve Block (TMNB) injection to decrease jaw muscle pain, overall pain, improve mouth opening and minimize pain medication consumption. 80 participants undergoing lower third molar removal under sedation will be enrolled. Those who develop significant jaw muscle pain on the following day will be randomized to receive either the TMNB injection or a placebo. Daily ecological momentary assessments (EMAs) will be collected reflecting elements of patient experience for all participants. On Day 8, participants return for an end-of-study evaluation and return their unused pain medications. Up to 40 participants who are randomized to receive TMNB/placebo will be recruited to participate in a qualitative interview regarding their experience.

Participants needed: 80
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Rutgers, The State University of New JerseyUpdated: Jun 18, 2026Locations: 1
Eligibility criteria

are 18 years or older, [+5]

Compromised ability to guard their self-interest, for e.g., prisoners, children,... [+4]

Status: Recruiting

Effects of TPR and Z Techniques on Pain and Drug Leakage in Intramuscular Injections

This randomized, triple-blind clinical trial compares the effectiveness of Z-track and TPR (traction-pressure-release) techniques in reducing pain and medication leakage during ventrogluteal intramuscular injections. Pain is measured using VAS, and leakage is assessed with a millimeter scale. The study aims to identify a more efficient, less painful injection method.

Participants needed: 76
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Cumhuriyet UniversityUpdated: Jun 4, 2025Locations: 2
Eligibility criteria

Aged 16-40 [+3]

Wounds, redness, bruising, tenderness, or stiffness at the injection site [+3]

Status: Not yet recruiting

An Bioequivalence Study of Loxoprofen Sodium Patches in Healthy Volunteers

This study was a single-center, randomized, open-label, two-agent, two-cycle, double-cross bioequivalence trial.

Participants needed: 40
Trial details
Phase: Phase 1Age: 18-65Biological sex: AllType: InterventionalSponsor: Frontier Biotechnologies Inc.Updated: Jul 19, 2024
Eligibility criteria

Male weight ≥50 kg, female weight ≥45 kg, body mass index (BMI) between 19.0 and... [+2]

Participated in other drug intervention studies within 90 days [+17]