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Pain clinical trials

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NCT ID: NCT03528668 Recruiting - Pain Clinical Trials

Patient Receptiveness to Using Virtual Reality

Start date: April 16, 2018
Phase:
Study type: Observational

This study will evaluate the acceptability, use, and general effect that exposure to virtual reality has on hospitalized patients reporting at least one discomfort including recent or current moderate-severe pain.

NCT ID: NCT03526055 Recruiting - Pain Clinical Trials

Evaluation of Conventional and Long Pulse Widths During a Temporary Spinal Cord Stimulation Trial

Start date: February 26, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effect of pulse widths <500 µS and >1000 µS on clinical outcomes during a temporary SCS trial.

NCT ID: NCT03520608 Recruiting - Clinical trials for Painful Diabetic Peripheral Neuropathy

Painful Diabetic Peripheral Neuropathy Study of Chinese OutPatiEnt

SCOPE
Start date: May 1, 2018
Phase:
Study type: Observational

Painful Diabetic peripheral Neuropathy Study of Chinese OutPatiEnt (PDN-SCOPE): a multi-center cross-sectional registry study of clinical characteristics and treatment survey of PDN in China

NCT ID: NCT03517644 Recruiting - Pain Clinical Trials

Investigating Hope and Expectations in Open-Label Placebos

I-HELP
Start date: February 10, 2018
Phase: N/A
Study type: Interventional

Research has shown that placebo effects contribute substantially to clinical outcomes. Recent evidence suggests that placebos remain effective even if they are openly described as placebos (so-called Open-Label Placebos). In this study, the investigators examine hope and expectations as components of open-label placebos in an experimental study investigating pain..

NCT ID: NCT03506763 Recruiting - Pain Clinical Trials

Effect of Pre-medication in Pain Measures on Office Hysteroscopy

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

Will be perform a RCT to compare pain measure on office hysteroscopy after pre-medication with oral analgesic. Patients will be alocate to oral sodic diclofenac, scopolamin or placebo. We will compare visual analog score of pain after the procedure. Patients: patients with indication of office hysteroscopy to evaluate uterine intracavitary abnormality. Interventions Group 1 (control) The patients will receive about 2 h prior to the procedure 2 placebo tablets. Group 2 (diclofenac + scopolamine) The patients will receive about 2 h prior to the procedure 1 tablet of diclofenac sodium 50 mg and 1 tablet of scopolamine 2 mg. Group 3 (diclofenac only). Patients will receive approximately 2 h prior to the procedure 1 tablet of diclofenac sodium 50 mg and 1 tablet of placebo.

NCT ID: NCT03504748 Recruiting - Pain Clinical Trials

Deep rTMS in Parkinson Disease Pain Syndromes

Start date: July 20, 2015
Phase: N/A
Study type: Interventional

Pain is the most prevalent non-motor symptom in Parkinson disease, and the motor improvement not always is related to the pain improvement with the medication treatment. By this, we are testing a non-invasive method called transcranial magnetic stimulation as an alternative to treat pain related to Parkinson disease. This technique can lead to either inhibitory or excitatory effects in brain circuits depending on stimulation parameters, and is known to provide analgesic effects.

NCT ID: NCT03496467 Recruiting - Pain Clinical Trials

Safety/Efficacy of Nepafenac Punctal Plug Delivery System Compared to Placebo to Control Ocular Pain/Inflammation After Cataract

Start date: March 5, 2018
Phase: Phase 2
Study type: Interventional

This is a Phase 2, multi-center, randomized, parallel-arm, double-masked, placebo-controlled study. One (1) to 2 days prior to their scheduled cataract surgery, each study subject will be randomized (2:1) in to one of two treatment groups: N-PPDS or p-PPDS, which are inserted in the lower punctum of the subject's scheduled surgical eye. All plugs will remain in the study subject's lower punctum for a period of 2 weeks following cataract surgery.

NCT ID: NCT03480724 Recruiting - Pain Clinical Trials

Assessing the Efficacy of Virtual Reality Analgesia (VRA) in Pediatric Patients for Pain Control

PEDSPAINVR
Start date: July 6, 2017
Phase: N/A
Study type: Interventional

To evaluate the efficacy of virtual reality analgesia (VRA) for pediatric patients undergoing Botulinum toxin injections (BTI) for spasticity management. Patients will be assigned to one of three groups; one group of subjects will randomly be assigned to VRA intervention using Google Cardboard Virtual reality head- mounted display powered by a iPod touch, a second group of subjects will receive VRA with Oculus Rift, and a third group of subjects will receive no intervention beyond standard sedation, anesthetic, and/or restraint—this group will serve as the control group.

NCT ID: NCT03479619 Recruiting - Clinical trials for Diabetes Mellitus, Type 2

Comparison of Three Lancing Devices Regarding Capillary Blood Volume and Lancing Pain Intensity.

Start date: March 6, 2018
Phase: N/A
Study type: Interventional

A randomized single-blind study with the use of three lancing devices equipped with personal lancets. Every device will be studied for three lancet sizes: 28G, 30G, and 33G with the minimum and maximum puncture depth setting.

NCT ID: NCT03475641 Recruiting - Pain Clinical Trials

Femoral Nerve Blockade in Endovenous Laser

Start date: March 13, 2017
Phase: N/A
Study type: Interventional

Varicose veins affect a majority of adult population in the western world. They decrease quality of life and may also cause venous ulcers. Therefore varicose vein treatments are justified. Currently endovenous thermal ablation is a treatment of choice for varicose veins. At the outpatient setting, however, treating both limbs at the same time may be painful to the patient especially, if simultaneous phlebectomies are performed. The study aims to evaluate, if femoral nerve blockade can significantly decrease pain during the procedure without prolonging the stay in the hospital.