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NCT03944629 · ClinicalTrials.gov registry record
Efficacy of Arnica Montana in Reducing Postoperative Edema and Pain
A clinical trial, sponsored by Tufts University.
- Completed
- Registry status
- 53
- Enrollment target
NCT03944629 is a clinical trial that has completed, run by Tufts University. The registered enrollment target is 53 participants.
The verdict
NCT03944629 has completed, sponsored by Tufts University.
- COMPLETED
- Registry status
- 53 participants
- Enrollment target
Study Summary
This study is a prospective, randomized, double-blinded, controlled, clinical trial that evaluates the efficacy of using high potency homeopathic Arnica montana (SinEcch™) during the perioperative period for decreasing swelling and pain after extraction of partial or full/complete bony impacted third molars. The study group will be comprised of subjects who will receive homeopathic Arnica montana (SinEcch™) for perioperative management of edema and pain. The control group will be comprised of subjects who will receive matching SinEcch™ placebo (sugar pill).
Interventions
- OTHER Placebo
- DRUG SinEcch
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 53 participants |
| Start Date | 2018-01-26 |
| Est. Completion | 2022-06-14 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03944629
The ClinicalTrials.gov registry entry for NCT03944629 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 53 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Tufts University, which has 163 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT03944629 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03944629 about?
NCT03944629 is a clinical study titled "Efficacy of Arnica Montana in Reducing Postoperative Edema and Pain". This study is a prospective, randomized, double-blinded, controlled, clinical trial that evaluates the efficacy of using high potency homeopathic Arnica montana (SinEcch™) during the perioperative period for decreasing swelling and pain after extraction of partial or full/complete bony impacted thir...
What is the current status of trial NCT03944629?
This trial is currently completed. The enrollment target is 53 participants. The study started on 2018-01-26. Estimated completion is 2022-06-14.
What interventions are being tested in trial NCT03944629?
The interventions under investigation include: Placebo (OTHER), SinEcch (DRUG).
Who is sponsoring clinical trial NCT03944629?
This trial is sponsored by Tufts University, which has 163 total clinical trials registered on ClinicalTrials.gov.
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