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Last Updated: November 2, 2024

CLINICAL TRIALS PROFILE FOR MEPIVACAINE HYDROCHLORIDE


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All Clinical Trials for mepivacaine hydrochloride

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00121329 ↗ 4% Intrauterine Lidocaine Infusion for Pain Management in First Trimester Abortions Completed Oregon Health and Science University N/A 1969-12-31 Recent studies have investigated the use of local anesthetics (i.e. lidocaine, mepivacaine) to lessen the pain experienced with minor gynecologic procedures such as endometrial biopsy and office hysteroscopy. Local anesthetic injected into the uterine cavity has been demonstrated effective in some studies at decreasing patient pain associated with these intrauterine procedures at an anesthetic concentration of at least 2%. Based on this evidence, we hypothesized that an intrauterine lidocaine infusion may reduce patient pain during first trimester abortions.
NCT00154167 ↗ Safety and Efficacy Study of NV-101 in Dental Patients Completed Novalar Pharmaceuticals, Inc. Phase 2 2003-02-01 The purpose of this study was: - to determine if NV-101 accelerates recovery from numbness compared to placebo - to evaluate safety of NV-101
NCT00567450 ↗ Ropivacaine Versus Ropivacaine Plus Mepivacaine for Sciatic Block Completed Centre Hospitalier Universitaire, Amiens Phase 4 2007-09-01 In loco regional anesthesia, much more than for general anesthesia, the choice of the product is largely left at the discretion of the practitioner. Two categories of local anesthetics are distinguished according to their pharmacodynamic characteristics: products with a short time of installation and a short duration period, and products with a longer delay of installation of the sensitive and motor block, but with a long-term duration. Indeed, the combined use of two products pharmacodynamically different seems to be of a practical interest. This study provides a comparison of the onset of action of 30 ml of ropivacaine 0.75% and 30ml of a mixture of ropivacaïne 0.75% associated with mepivacaïne 1.5% for the subgluteal sciatic nerve block. This is a prospective randomized double-blind study where the main criterion of judgment is the time of installation of a sensitive block compatible with surgery in the sciatic territory nerve. Fifteen patients per group were calculated to detect a 50% decrease of the onset of action in the combination group with a power of 90% and alpha to 5%, according to a previous pilot study. The secondary endpoints are the intensity and time of installation of the motor block, the duration of sensitive and motor block, the total dose of morphine administered within 48 hours, as well as its possible side effects.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for mepivacaine hydrochloride

Condition Name

Condition Name for mepivacaine hydrochloride
Intervention Trials
Symptomatic Irreversible Pulpitis 8
Pain 7
Anesthesia 4
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Condition MeSH

Condition MeSH for mepivacaine hydrochloride
Intervention Trials
Pulpitis 14
Pain, Postoperative 9
Osteoarthritis, Hip 3
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Clinical Trial Locations for mepivacaine hydrochloride

Trials by Country

Trials by Country for mepivacaine hydrochloride
Location Trials
United States 23
Egypt 8
Brazil 7
Spain 4
Italy 4
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Trials by US State

Trials by US State for mepivacaine hydrochloride
Location Trials
Massachusetts 2
Minnesota 2
North Carolina 2
Tennessee 2
Pennsylvania 2
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Clinical Trial Progress for mepivacaine hydrochloride

Clinical Trial Phase

Clinical Trial Phase for mepivacaine hydrochloride
Clinical Trial Phase Trials
Phase 4 31
Phase 3 7
Phase 2/Phase 3 5
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Clinical Trial Status

Clinical Trial Status for mepivacaine hydrochloride
Clinical Trial Phase Trials
Completed 52
Not yet recruiting 11
Unknown status 8
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Clinical Trial Sponsors for mepivacaine hydrochloride

Sponsor Name

Sponsor Name for mepivacaine hydrochloride
Sponsor Trials
Cairo University 12
University of Sao Paulo 4
Duke University 2
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Sponsor Type

Sponsor Type for mepivacaine hydrochloride
Sponsor Trials
Other 100
Industry 3
U.S. Fed 1
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