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NCT01620112
The Effects of Different Clonidine Concentrations on Axillary Brachial Plexus Block With 1,5% Lidocaine for Upper Limb Surgery: a Prospective Randomized Study
Phase 2 trial testing high Clonidine concentration in Fascicular Block in 60 participants. Completed in 1 July 2011.
1 July 2011
Quick facts
| Lead sponsor | Universidade Federal do Rio de Janeiro |
|---|---|
| Phase | Phase 2 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 60 |
| Start date | 1 February 2009 |
| Primary completion | 1 July 2011 |
| Estimated completion | 1 July 2011 |
Drugs / interventions tested
- high Clonidine concentration — full drug profile →
- low clonidine concentration — full drug profile →
- Lidocaine — full drug profile →
- Lidocaine 40 ml — full drug profile →
Conditions studied
- Fascicular Block — all drugs for Fascicular Block →
- Motor Activity — all drugs for Motor Activity →
- Pain, Postoperative — all drugs for Pain, Postoperative →
- Latency Period — all drugs for Latency Period →
Sponsor
Universidade Federal do Rio de Janeiro — full company profile →
Who can join
Adults 18 to 65, any sex, with Fascicular Block or Motor Activity. Patients with the condition only — healthy volunteers not accepted.
What's being measured
Primary outcomes are the specific endpoints the trial is designed to prove or disprove.
-
sensorial and motor block duration
Time frame: 24 hours after surgery
to compare two concentrations of clonidine on different volumes of lidocaine, in terms of sensorial and motor block duration
Sponsor's own description
The purpose of this study is to determine whether different clonidine concentration on axillary brachial plexus block with 1,5% lidocaine for upper limb surgery may influence the sensory and motor block onset time and duration, postoperative analgesia duration, postoperative pain intensity
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT01620112
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other Universidade Federal do Rio de Janeiro trials
Trials by the same sponsor.
- NCT07584564 — Application of the Concept of Proprioceptive Neuromuscular Facilitation in Trunk Control in Patients Admitted to the ICU · NA · not yet recruiting
- NCT07062497 — Clonidine in Ultrasound-guided Rectus Sheath Block for Outpatient Umbilical Hernioplasty · Phase 2, PHASE3 · recruiting
- NCT07191743 — Functional Assessment in Critically Ill Patients · recruiting
- NCT06733714 — Association of Transcranial Alternating Current Stimulation with Digital Cognitive Training for Cognitive Remediation in · NA · recruiting
- NCT07391943 — Self-Guided CBT Mobile App for Treatment-Resistant Panic Disorder (CBT) Cognitive Behavioral Therapy · 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 NCT01620112 (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 Universidade Federal do Rio de Janeiro
- Last refreshed: 14 June 2012
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/NCT01620112.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing