Clinical Trials Logo

Pain clinical trials

View clinical trials related to Pain.

Filter by:

NCT ID: NCT02821390 Completed - Pain Clinical Trials

Effect of Topical Nepafenac 0.1% on Pain Related to Intravitreal Injections

Start date: June 2016
Phase: N/A
Study type: Interventional

The analgesic effect of Nepafenac 0.1% Ophthalmic Drops on ocular pain related to intravitreal injections will be evaluated. Pain perception will be assessed by the Short Form of the McGill Pain Questionnaire.

NCT ID: NCT02821169 Completed - Pain Clinical Trials

Infiltration in the Region of the Palatine Ganglion Spheno by Ropivacaine on Postoperative Pain

ROPI_POSTOP
Start date: April 2015
Phase: Phase 3
Study type: Interventional

Endoscopic sinus surgery (ESS) is a prevalent surgical procedure. It is required in many chronic rhinosinusitis for whom the medical treatment failed. In order to improve the postoperative management of patients treated with ESS, we aim to assess the analgesic action of local injection of ropivacaine in the nasal fossa.

NCT ID: NCT02816996 Completed - Pain Clinical Trials

Patient Comfort During Dermatologic Procedures

Start date: January 24, 2017
Phase: N/A
Study type: Interventional

The goal of this study is to find the effect of holding a patient's hand on anxiety and pain during dermatologic procedures.

NCT ID: NCT02815189 Completed - Pain Clinical Trials

Incidence of Flare-ups and Apical Healing After Single-visit or Two-visits Treatment.

FlareUp
Start date: February 2014
Phase: Phase 2
Study type: Interventional

Aim to compare Incidence of flare-ups and apical healing after single-visit or two-visits treatment of teeth with necrotic pulp and apical periodontitis after a two-year control period. 110 teeth with a diagnosis of pulp necrosis and apical radiolucency at the apex. Working length was established with EAL and confirmed radiographically. M4 system with Flex-R files were used to complete canal preparation. Level of discomfort were recorded and cases with severe postoperative pain and/or swelling were classified as flare-ups.

NCT ID: NCT02812381 Completed - Pain Clinical Trials

Efficacy of Neuromuscular Bandage Technique Against Jones Technique After the Supraespinatus Muscle Tendon Suture

Start date: July 2016
Phase: N/A
Study type: Interventional

The suture of the supraspinatus tendon is a common surgery that requires physical therapy for back pain and functional impairment to such surgery. Kinesiotaping technique (KT) is being used to treat myofascial trigger points that appear after surgery and for the treatment of physiotherapy in the supraspinatus muscle and deltoid. To evaluate the effectiveness of KT technique over the technique of Jones (Straincounterstrain or SCS) in patients undergoing suture the tendon of the supraspinatus muscle.

NCT ID: NCT02809144 Completed - Pain Clinical Trials

A Novel Combination of Peripheral Nerve Blocks for Patients Scheduled for Shoulder Surgery

Start date: April 2016
Phase: N/A
Study type: Interventional

Interscalene block has been the traditional regional anesthesia for shoulder surgery and postoperative pain. However, the risk of phrenic nerve palsy and irreversible nerve injury have encouraged search for alternative methods.

NCT ID: NCT02808637 Completed - Pain Clinical Trials

Vaccine‐Related Pain in Infants

Start date: April 2015
Phase: N/A
Study type: Interventional

This is a randomized double-blind controlled study and was performed to compare effects of rapid injection without aspiration and 10-second manual pressure before injection on pain severity and crying time in 4-6-month-old infants given the vaccine DTaP/IPV/Hib. The study population included all the infants presenting for DTaP/IPV/Hib to two family health centers between April and August in 2015. The study sample included 128 infants based on confidence interval of 95% and statistical power of 80%. The sample was divided into four groups; i.e. manual pressure, rapid injection without aspiration, manual pressure combined with rapid injection without aspiration and control groups. There were 32 infants in each group. Gender was adjusted in all groups. Stratified and block randomizations were used.

NCT ID: NCT02806609 Completed - Pain Clinical Trials

Effect of Muscle Pain in Late Cold Water Immersion, Muscular Recruitment, Postural Control Dynamic and Sleep Quality

Start date: June 1, 2016
Phase: N/A
Study type: Interventional

Objective: To evaluate the effect of cold water immersion in elayed onset muscle soreness, muscle recruitment, dynamic postural control and quality of sleep in young soccer players. Methods: The sample will consist of 28 soccer players between 18 and 21 years of the same football club and with the same routine practices and games. At first athletes will respond to the IC and will be submitted to the test of a repetition maximum. After three days the athletes will analysis of muscle recruitment by electromyography and dynamic posture control through the force platform both during the time of shooting, moreover, will respond to scale the quality of sleep the previous night and one on pain, then they are instructed to perform a fatigue protocol for the quadriceps and then will be randomized to one of four intervention groups: cold water immersion, submersion in water at room temperature, or active recovery control. The same APPRAISAL be remade into three new moments, 24, 48 and 72 hours after the fatigue test. Hypothesis: The variables will be considered: Pain intensity in the quadriceps muscle, quality of sleep the night after intervention protocol, electromyographic analysis of the rectus femoris, vastus medialis oblique and vastus lateralis at the time of shooting, as well as postural control when the shot off. It is intended to establish the best way of recovery of late quadriceps muscle pain and contribute to the clinical practice of active recovery or rest in young soccer players.

NCT ID: NCT02806323 Completed - Clinical trials for Neck Pain Musculoskeletal

Individually Tailored Yoga Program for the Treatment of Chronic Neck and Back Pain

Start date: July 1, 2016
Phase: N/A
Study type: Interventional

The goal of this pilot study is to determine the feasibility of an individually tailored yoga program delivered in a group setting for the treatment of chronic neck and back pain in a low income population. Chronic pain is one of the most common, costly, and disabling conditions, and is often refractory to treatment. Yoga is a promising treatment for chronic pain. This pilot study will test the hypothesis that study subjects will participate in a voluntary 12 week yoga intervention for the treatment of chronic neck and back pain, as assessed by attendance at 12 weekly yoga practice sessions. Secondary outcomes will include change in pain and quality of life scores over the 12 week study period as assessed by the Visual Analog Scale for Pain Severity and EQ-5D-3L.

NCT ID: NCT02804477 Completed - Chronic Cancer Pain Clinical Trials

Validation and Assessment of Patient Adherence to Opioids for Cancer Pain Using MMAS 8 Pain Clinic

Start date: June 2016
Phase: N/A
Study type: Observational

This study aims at finding degree of adherence of patients to their chronic pain medication prescriptions containing opioid e.g. Morphine, using Morisky Medication Adherence Scale 8, self- reported questionnaire. Also relationship of various demographic, disease related and opioid related factors to medication adherence.