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Anesthesia, Local clinical trials

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NCT ID: NCT03137615 Completed - Anesthesia, Local Clinical Trials

The Cardiovascular Changes Associated With Septal Local Anaesthesia

Start date: November 2014
Phase: N/A
Study type: Observational

The purpose of this study is to determine the effects on the heart of injecting local anaesthetic into the nose prior to surgery on the pituitary gland?

NCT ID: NCT03130855 Not yet recruiting - Anesthesia, Local Clinical Trials

Comparison Between Efficiency of Inferior Alveolar Nerve Block and Buccal Infiltration Techniques Using Articaine 4% 1:100000

Start date: May 15, 2017
Phase: N/A
Study type: Interventional

This split mouth randomized control trial is designed as to compare the effectiveness of the buccal infiltration technique with the gold standard inferior alveolar nerve block in anesthetizing mandibular second primary molars to undergoing pulpal treatment. patient will be videotaped during pulpal treatment of their teeth and an accessing pain will be through an objective pain scale (SEM scale), (sound-eye-motor scale). the patient will be asked to fill in a subjective Wong Baker pain scale for the pain suffered during injecting the local anesthetic agent in both techniques.

NCT ID: NCT03127943 Completed - Anesthesia, Local Clinical Trials

Clinical Outcomes Mandible: Buffered 1% vs. Non-Buffered 1% Lidocaine

Start date: May 1, 2017
Phase: Phase 4
Study type: Interventional

Assess the clinical impact of Buffered 1% lidocaine with epinephrine as compared to the Non-buffered 1% lidocaine with epinephrine in dental and oral surgical procedures.

NCT ID: NCT03117140 Completed - Anesthesia, Local Clinical Trials

Analgesia Duration of Dexamethasone, Buprenorphine, or Clonidine With Ropivacaine for Interscalene Nerve Block

Start date: December 2013
Phase: Phase 4
Study type: Interventional

This is a prospective randomized controlled triple-masked study looking at the duration of nerve block analgesia when using the listed adjuvants (dexamethasone, buprenorphine and clonidine) plus ropivacaine versus plain ropivacaine alone.

NCT ID: NCT03111342 Completed - Pain, Acute Clinical Trials

Intracervical Anesthesia and Pain Associated With Intrauterine Contraceptive Insertion

Start date: June 1, 2017
Phase: Phase 4
Study type: Interventional

The primary aim of our study is to evaluate the effect of intracervical anesthesia on pain scores immediately following levonorgestrel-releasing intrauterine system (LNG-IUS) insertion in nulligravida women.

NCT ID: NCT03091049 Completed - Anesthesia, Local Clinical Trials

RAOLA Observational: Local Anesthesia During Cardiac Catheterization

Start date: November 1, 2014
Phase:
Study type: Observational

An open label observational clinical study to compare the efficacy of EMLA cream (lidocaine 2.5% and prilocaine 2.5% in a ratio of 1:1 by weight) in comparison to the established local anesthesia (LA) protocol of lidocaine subcutaneous injection, in providing adequate peri-operative local anesthesia during transradial coronary angiography

NCT ID: NCT03072394 Recruiting - Clinical trials for Coronary Artery Disease

Local Anesthesia in Radial Catheterization

RAOLA
Start date: January 10, 2015
Phase: Phase 4
Study type: Interventional

A randomized clinical trial to test the efficacy of EMLA cream (lidocaine 2.5% and prilocaine 2.5% in a ratio of 1:1 by weight) in comparison to the established local anesthesia (LA) protocol of lidocaine subcutaneous injection, in providing adequate peri-operative local anesthesia during transradial coronary angiography.

NCT ID: NCT03016117 Completed - Anesthesia, Local Clinical Trials

Anesthetic Efficacy of PECS II Block and Parasternal Block

Start date: March 15, 2017
Phase: N/A
Study type: Interventional

The study evaluate the anesthetic efficacy of Pecs II block II and parasternal block during quadrantectomy with or without axillary dissection, in breast cancer surgery

NCT ID: NCT02995291 Completed - Anesthesia, Local Clinical Trials

Reversing the Effects of 0.5% Bupivacaine

Start date: February 10, 2017
Phase: Phase 4
Study type: Interventional

Clinical trials have shown phentolamine mesylate (PM), brand name OraVerse, to be effective at reducing the amount of time to reversal of local anesthesia with different dental anesthetics. However, to date no study investigated the efficacy of phentolamine mesylate to reverse anesthesia induced with the use of Bupivacaine. The objective of the proposed research is to conduct a pilot-scale randomized clinical trial evaluating the difference in time required for the return of normal soft-tissue sensation and function in participants who have received 0.5% Bupivacaine HCl, 1:200,000 epinephrine, followed by an injection with either 1) OraVerse (phentolamine mesylate) or 2) sterile physiological water (control).

NCT ID: NCT02988219 Recruiting - Surgery Clinical Trials

Cardiac Arrhythmias in Patients Undergoing Kidney Cancer Surgery Depending on the Anaesthesia Method

Start date: June 2010
Phase: Phase 4
Study type: Interventional

This study evaluates the incidence of cardiac arrhythmias during the perioperative period in patients undergoing open kidney cancer surgery in the lateral position. All the participants will be randomly allocated to receive general (Group G) or combined epidural/general anaesthesia (Group G/E). The anaesthetic technique is standardized. The Holter monitor will be applied at the evening before the surgery, tracing continuously for a period of 24 hours (7PM-7PM)