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NCT ID: NCT03431636 Not yet recruiting - Pain Clinical Trials

Effect of Different Techniques of Recovery in Para-athletes

Start date: July 25, 2020
Phase: N/A
Study type: Interventional

Para-athletes are submitted and intense efforts in training and competitions that often overlap in days and weeks. In this sense, and in the search for better brands and indexes, it is necessary to use recovery methods that allow less late muscle pain and better physical performance. Recovery methods are widely used in athletes of various modalities, however there are no studies that point out their effects on para-athletes. This highlights the need for studies on this topic. Paragliding athletes, who train at the Londrina Yacht Club, Londrina Canoeing and Rowing School, who present paraplegia after spinal cord injury, with motor level T10 or lower, without any problem of thermoregulation will participate in the study. All were male and female, with no complaints of musculoskeletal pain or history of upper limb muscle injuries in the last six months and with the same demand for training and competitions. Initially an evaluation will be performed where 1RM, VO2 max, pain, spasticity, body temperature, heart rate variability and electromyographic signal of the involved muscles will be tested. After three days they will be induced to fatigue through a protocol in the traction exercise and immediately directed to one of the 3 intervention groups: ice pack, immersion in cold water or rest. The same baseline evaluations will be repeated after 24, 48 and 72 hours. It is expected that the group submitted to immersion in cold water presents better parameters for pain and sports performance.

NCT ID: NCT03373513 Not yet recruiting - Pain Clinical Trials

Robotic-assisted Hysterectomy: Single- vs. Multi-port Laparoscopic Access

Start date: February 1, 2019
Phase: N/A
Study type: Interventional

robotic single site surgery (R-SSH) is a novel technique, which may be superior to conventional multiport hysterectomy in select patients regarding cosmesis and postoperative pain. We, perform a randomized trial to compare R-SSH with multiport laparoscopic hysterectomy with regard to the postoperative rehabilitation, cosmesis, the operational cost, and the perioperative morbidity.

NCT ID: NCT03312153 Not yet recruiting - Pain Clinical Trials

Effect of Neem and NaOCl on Postoperative Pain and Amount of Endotoxins

Start date: August 1, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to compare the effect of Neem (azadirachta indica) and 2.5% sodium hypochlorite as root canal irrigants on the intensity of post-operative pain and the amount of endotoxins in necrotic teeth.

NCT ID: NCT03282110 Not yet recruiting - Pain Clinical Trials

Comprehensive Acupuncture for Depressive Disorder With Comorbid Psychogenic Pain

Start date: November 30, 2017
Phase: Early Phase 1
Study type: Interventional

Experimental and clinical studies have indicated that acupuncture has a good effect for depression and comorbid pain. The purpose of this research is to compare the effect of comprehensive electro-acupuncture therapy and western medicine citalopram for for depressive disorder with comorbid psychogenic pain. This research is a assessor blinded, randomized controlled trials. 60 patients will be randomly divided into comprehensive electro-acupuncture group and western medicine citalopram for 8 weeks treatment and the therapeutic effect is done at the end of 1,2,4,6,8 week.

NCT ID: NCT03275233 Not yet recruiting - Clinical trials for Painful Peripheral Neuropathy

Psychiatric Comorbidities in Patients With Painful Peripheral Neuropathy

Start date: September 4, 2019
Phase:
Study type: Observational

Psychiatric comorbidities in patient with Painful Peripheral neuropathy

NCT ID: NCT03228628 Not yet recruiting - Pain Clinical Trials

Nitrous Oxide for Lumbar Puncture

NO for LP
Start date: October 1, 2017
Phase: Phase 4
Study type: Interventional

Lumbar puncture (LP) is a frequent exam that can cause pain and anxiety. In a pilot single-center study, it has been shown that nitrous oxide use during the procedure was able to reduce both pain and anxiety (Moisset et al., Eur J Neurol 2017). The goal of this multi-center trial is to confirm these results in a larger and more heterogeneous group of patients having a LP.

NCT ID: NCT03190187 Not yet recruiting - Pain Clinical Trials

Spinal Manipulation Effectiveness in Spinal Disorders

Start date: February 20, 2018
Phase: N/A
Study type: Interventional

The aim of the present intervention study is to determine the effectiveness of manipulation techniques.

NCT ID: NCT03117075 Not yet recruiting - Pain Clinical Trials

The Efficacy of Pain Management With Self-reporting Pain Monitoring System in Cancer Patient

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

To compare the pain scales between clinician evaluated and reported with wearable device by patients.

NCT ID: NCT03075293 Not yet recruiting - Pain Clinical Trials

Pain Management of Children With Appendicitis in the Emergency Department (ER)

Start date: March 26, 2017
Phase: N/A
Study type: Observational

The aim of this retrospective study is to determine the percentage of children with appendicitis who were given analgesics or opioids in the ER, to reduce their pain.

NCT ID: NCT02972229 Not yet recruiting - Pain Clinical Trials

Whole Versus Partial Vertebral Body IMRT for Spinal Metastases

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

To compare the treatment effect and toxicity between Intensity-Modulated Radiation therapy for whole metastatic vertebral body and simple metastatic lesions of vertebra in metastatic spinal tumors