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NCT00713674: SJMRSA
Comparison of Decolonization of MRSA Using Theraworx
NA trial testing Theraworx in Methicillin-Resistant Staphylococcus Aureus. Withdrawn.
1 February 2009
Quick facts
| Lead sponsor | Mercy Research |
|---|---|
| Phase | NA |
| Status | Withdrawn |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Start date | 1 March 2008 |
| Primary completion | 1 February 2009 |
| Estimated completion | 1 February 2009 |
Drugs / interventions tested
- Theraworx — full drug profile →
- mupirocin antibiotic ointment — full drug profile →
Conditions studied
- Methicillin-Resistant Staphylococcus Aureus — all drugs for Methicillin-Resistant Staphylococcus Aureus →
Sponsor
Mercy Research — full company profile →
Who can join
18 and older, any sex, with Methicillin-Resistant Staphylococcus Aureus. Healthy volunteers can join.
What's being measured
Primary outcomes are the specific endpoints the trial is designed to prove or disprove.
-
Evidence of decolonization confirmed by intranasal culture
Time frame: Up to 14 days post treatment (+/- 1-2 days)
Sponsor's own description
The purpose of this study is to examine treatment method of Methicillin-resistant Staphylococcus aureus (MRSA) decolonization in patients.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT00713674
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Theraworx
Trials testing the same drug.
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- NCT03159260 — Effect of Theraworx/[pH]Uel on Night-time Leg Cramps and Spasm Symptoms · NA · completed
Other Mercy Research trials
Trials by the same sponsor.
- NCT04202718 — VitalConnect VitalPatch ECG Interpretation/Arrhythmia Detection · NA · withdrawn
- NCT04137770 — Application of the ICE-T Postoperative Multimodal Pain Regimen to Laparoscopic Hysterectomy · NA · terminated
- NCT03956082 — Ultravision™ System to Facilitate Low Impact Laparoscopic Surgery for Endometriosis · NA · completed
- NCT03634306 — Ultravision Visual Clearing System in Laparoscopic Hysterectomy and Myomectomy · NA · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT00713674 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Mercy Research
- Last refreshed: 21 March 2017
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00713674.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing