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Last Updated: April 23, 2024

CLINICAL TRIALS PROFILE FOR DURACLON


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All Clinical Trials for DURACLON

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00349921 ↗ Clonidine Versus Adenosine to Treat Neuropathic Pain Completed National Institute of Neurological Disorders and Stroke (NINDS) Phase 2 2004-08-01 The purpose of this study is to determine the effects of clonidine and adenosine on nerve pain.
NCT00349921 ↗ Clonidine Versus Adenosine to Treat Neuropathic Pain Completed Wake Forest School of Medicine Phase 2 2004-08-01 The purpose of this study is to determine the effects of clonidine and adenosine on nerve pain.
NCT00349921 ↗ Clonidine Versus Adenosine to Treat Neuropathic Pain Completed Wake Forest University Health Sciences Phase 2 2004-08-01 The purpose of this study is to determine the effects of clonidine and adenosine on nerve pain.
NCT00510016 ↗ Clonidine as Adjunct Therapy for the Treatment of Neonatal Abstinence Syndrome Completed Johns Hopkins University Phase 2 2002-07-01 To test the hypothesis that the combination of the tincture of opium (DTO) and clonidine will be more effective in treating infants with neonatal abstinence syndrome (opioid withdrawal) than tincture of opium (DTO) alone.
NCT00510016 ↗ Clonidine as Adjunct Therapy for the Treatment of Neonatal Abstinence Syndrome Completed National Institute on Drug Abuse (NIDA) Phase 2 2002-07-01 To test the hypothesis that the combination of the tincture of opium (DTO) and clonidine will be more effective in treating infants with neonatal abstinence syndrome (opioid withdrawal) than tincture of opium (DTO) alone.
NCT00678379 ↗ Pediatric Tonsillectomy Pain Reduction Study Completed Vanderbilt University Medical Center Phase 3 2008-04-01 Tonsillectomy is associated with a significant decrease quality of life in children secondary to pain, which is worsened with swallowing. The objective of the current study is to conduct a prospective, double-blind, placebo-controlled, randomized clinical trial using a pre-tonsillectomy infiltration of the tonsillar fossa comparing three treatment regimens in reducing post-tonsillectomy morbidity (i.e. pain, poor oral intake): 1) Placebo (saline injection) 2) bupivacaine (0.5%) + lidocaine (1%), 3) bupivacaine (0.5%) + lidocaine (1%) + clonidine (25 µg).
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for DURACLON

Condition Name

Condition Name for DURACLON
Intervention Trials
Neonatal Abstinence Syndrome 2
Postoperative Pain 2
Total Hip Arthroplasty 1
Total Knee Arthroplasty 1
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Condition MeSH

Condition MeSH for DURACLON
Intervention Trials
Neonatal Abstinence Syndrome 2
Pain, Postoperative 2
Syndrome 1
Neuralgia 1
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Clinical Trial Locations for DURACLON

Trials by Country

Trials by Country for DURACLON
Location Trials
United States 7
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Trials by US State

Trials by US State for DURACLON
Location Trials
Maryland 3
Pennsylvania 1
New York 1
Tennessee 1
North Carolina 1
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Clinical Trial Progress for DURACLON

Clinical Trial Phase

Clinical Trial Phase for DURACLON
Clinical Trial Phase Trials
Phase 4 3
Phase 3 1
Phase 2/Phase 3 1
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Clinical Trial Status

Clinical Trial Status for DURACLON
Clinical Trial Phase Trials
Completed 6
Terminated 2
Withdrawn 1
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Clinical Trial Sponsors for DURACLON

Sponsor Name

Sponsor Name for DURACLON
Sponsor Trials
Johns Hopkins University 3
National Institute on Drug Abuse (NIDA) 2
Gauda, Estelle B., M.D. 2
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Sponsor Type

Sponsor Type for DURACLON
Sponsor Trials
Other 14
NIH 3
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