Clinical Trials Logo

Paresthesia clinical trials

View clinical trials related to Paresthesia.

Filter by:
  • Completed  
  • Page 1 ·  Next »

NCT ID: NCT06251882 Completed - Clinical trials for Meralgia Paresthetica

Efficacy of Ultrasound-guided Injection of 5% Dextrose for Meralgia Paresthesia

Start date: January 1, 2022
Phase: N/A
Study type: Interventional

Meralgia paresthetica (MP) is one of the most common peripheral entrapment neuropathies of the lower limbs. It is characterized by paresthesia, pain, tingling, numbness, hypersensitivity, or other abnormal skin sensations on the anterolateral aspect of the thigh. The condition results from compression of the lateral femoral cutaneous nerve (LFCN) along its course, often occurring as the nerve exits the pelvis.The injection of 5% dextrose (D5W) under ultrasound guidance is a novel treatment method for peripheral nerve entrapment. However, there is limited evidence about the efficacy of this method for patients with MP. The investigators found D5W was more safe and effective than corticosteroids for patients with MP. Thus, this study aimed to evaluate the 6-month efficacy of ultrasound-guided injection of D5W for MP patients.

NCT ID: NCT05811741 Completed - Alveolar Bone Loss Clinical Trials

Impact of Mandibular Canal Trajectory on Paresthesia After Inferior Alveolar Nerve Lateralization

Start date: June 1, 2016
Phase:
Study type: Observational

This prospective cohort study aims to investigate the relationship between mandibular canal trajectory and the duration of postoperative paresthesia in patients undergoing inferior alveolar nerve lateralization. The study will assess mandibular canal trajectory using anatomic factors and evaluate nerve sensory function using subjective and objective tests. Implant success criteria will also be assessed. The study will be conducted on patients who underwent IANL due to mandibular atrophy and were unable to receive standard or short implant placement. Data will be collected at regular follow-up visits up to 1-year post-surgery.

NCT ID: NCT05744882 Completed - Clinical trials for Impacted Third Molar Tooth

The Need Of Root Canal Treatment After Coronectomy In Mandibular Third Molars

Start date: January 1, 2021
Phase: N/A
Study type: Interventional

The study included 24 patients with written and verbal consent Results with close proximity to IAN diagnosed based on radiographs and evaluation on the criteria of Howe, and Poyton were selected and divided into two groups by lottery method into coronectomy and coronectomy with root canal treatment following coronectomy groups. Patients were re-evaluated on three weeks for complications and three months follow-ups for radiographic evaluations of root-fragment migration

NCT ID: NCT05319275 Completed - Paresthesia Clinical Trials

Study of Acetyllevocarnitine Hydrochloride Tablets in Chinese Patients With Paresthesias Caused by DPN

Start date: July 23, 2020
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the efficacy of Acetyllevocarnitine Hydrochloride Tablets compared with placebo after 24 weeks, in chinese patients with paresthesia caused by Diabetic Peripheral Neuropathy (DPN).

NCT ID: NCT05205616 Completed - Fracture Clinical Trials

Trial of Bilateral Sagittal Split Osteotomy Induced Paresthesia Using Ultrasonic vs. Reciprocating Saw Instrumentation

Start date: July 20, 2021
Phase: N/A
Study type: Interventional

The aim of this prospective study is to analyze the postoperative paresthesias experienced in patients who undergo bilateral sagittal split osteotomies (BSSO) using an ultrasonic saw, versus a reciprocating saw. Patients included in the study are ages 15-45 scheduled to undergo BSSO surgery at the University of California, San Francisco. One side of the patient's mandible will be instrumented with either the Stryker Sonopet ultrasonic saw or traditional reciprocating saw, while the other side will receive the remaining intervention (determined via randomization on the day of surgery). Patient paresthesias will then be analyzed on each side for 3 months postoperatively (at postoperative days: 1, 7, 14, 28, and 84). Sensory examinations will be carried out by blinded examiners using von Frey hairs and two point discrimination testing. Patients will also subjectively rate their sensation on each side. The results will then be analyzed to determine if patient paresthesias, including the severity and duration, differed depending on which instrument was used, the ultrasonic or reciprocating saw.

NCT ID: NCT04747119 Completed - Clinical trials for Meralgia Paresthetica

Effect of MET on Meralgia Paraesthesia Postpartum "Muscle Energy Technique"

MET
Start date: October 1, 2020
Phase: N/A
Study type: Interventional

To investigate the effect of muscle energy technique on Femoral meralgia paraesthesia in a postpartum female. BACKGROUND: meralgia paraesthesia is one of the serious disorders in the postpartum female which results in pain and less physical activities. ………HYPOTHESES: This study hypothesized that: muscle energy technique will have a significant effect on Femoral meralgia paraesthesia in postpartum female

NCT ID: NCT02986074 Completed - Chronic Pain Clinical Trials

CompaRison of Paresthesia Mapping to anatomIc Midline-based burSt Programming Strategies

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

The study will compare therapeutic efficacy of a novel spinal cord stimulation leads implant based on anatomical landmarks with standard surgical implantation technique.

NCT ID: NCT01205464 Completed - Fatigue Clinical Trials

Effects of Doxycycline on Persistent Symptoms Post-neuroborreliosis

Start date: February 2005
Phase: N/A
Study type: Interventional

The aim of this randomised, double-blind crossover study was to determine whether Doxycycline has an impact on the persistent symptoms post-neuroborreliosis, through alterations in the immune response and whether such an effect could influence the clinical outcome.

NCT ID: NCT00800527 Completed - Chest Pain Clinical Trials

Efficacy of Gabapentin in the Treatment of Chest Pain and Paresthesia in Patients With Sternotomy

Start date: November 2007
Phase: Phase 4
Study type: Interventional

In this study, the investigators aim to demonstrate the efficacy of gabapentin compared with diclofenac in the treatment of chronic non-ischemic chest pain and paresthesia of the patients with sternotomy and to elucidate the similarities of PCPP to neuropathic pain syndromes.

NCT ID: NCT00746694 Completed - Breast Neoplasms Clinical Trials

A Study to Determine the Management of Palmar-plantar Erythrodysesthesia (PPE) in Patients With Metastatic Ovarian or Breast Cancer Treated With Caelyx (Study P05020)

Start date: October 2007
Phase: N/A
Study type: Observational

The objective of this trial is to study the management of PPE in participants with metastatic ovarian or breast cancer treated with Caelyx, and determine the frequency of use of pharmacological treatment (preventive or therapeutic) for PPE and compliance of educational recommendations for PPE.