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NCT ID: NCT05868460 Recruiting - Clinical trials for Temporomandibular Joint Disorders

Laser Therapy on TMJ Disorders After Head and Neck Cancer.

Start date: May 21, 2023
Phase: N/A
Study type: Interventional

Temporomandibular disorder (TMD) is a term describing musculoskeletal conditions of the face, jaw and temporal regions. TMD is frequently associated with pain and/or dysfunction such as impaired jaw function, pain in the temporomandibular joint (TMJ), muscles and/or related structures, and associated headaches. The aetiology of TMD is multifactorial and complex.

NCT ID: NCT05867459 Recruiting - CKD PREGNANT WOMEN Clinical Trials

Maternal and Fetal Outcome of CKD Mother Patient in Sohag Governorate

Start date: April 1, 2023
Phase:
Study type: Observational

Aim of the work: In this study, we aimed: Is to investigate the following issues: (1) the pregnancy outcomes of patients with CKD (2) additional risk factors for adverse pregnancy outcomes in patients with CKD in the area of sohag governorate.

NCT ID: NCT05865145 Recruiting - Elderly Clinical Trials

Effects of Aerobic Exercise on Basic Metabolic Panel Perceived Exertion and Exercise Adherence in Elderly

Start date: May 2023
Phase: N/A
Study type: Interventional

Participants were randomly assigned to two groups prior to their second visit: the High intensity interval training group A (HIIT) and Low intensity interval training group B (LIIT). The randomization processes were conducted in Excel utilizing a random-number generator. Prior to the second visit, each participants' target exercise heart rate ranges were determined. Group A will receive a program of high intensity interval training program Group B will receive a program of Low intensity interval training program

NCT ID: NCT05864989 Recruiting - Periodontitis Clinical Trials

Non-Incised Papilla Flap in Deep Supraossous Defects

Start date: April 1, 2023
Phase: N/A
Study type: Interventional

The objective of this study was to assess the effectiveness of NIPSA in periodontal lesions with deep supra-alveolar defects, measuring the clinical efficacy of this flap. The non-incised papilla surgical approach (NIPSA) is a novel technique that accesses the periodontal defect from apical direction and was established with the aim of creating clinical advances compared with marginal access techniques. The defects with a supra-alveolar components are more frequent than intrabony defects, there is very little evidence about their treatment .

NCT ID: NCT05864183 Recruiting - PreDiabetes Clinical Trials

Screening for Risk Factors of Prediabetes Among Adult Patients at Sohag University Hospital

Start date: April 15, 2023
Phase:
Study type: Observational [Patient Registry]

- Prediabetes is an intermediate state of hyperglycemia with glycemic parameters above normal but below the diabetes threshold.. - during the average 3 years of follow-up Prediabetes is diagnosed based on laboratory tests: fasting plasma glucose level (100-125 mg/dl) ;HbA1c, (5.7-6.4%) or plasma glucose level after an oral glucose tolerance test ( 140-199 mg/dl). - Reports estimate that more than 470 million people will have prediabetes by 2030. - According to an expert panel of the American Diabetes Association, up to 70% of individuals with prediabetes will eventually develop diabetes. - Observational evidence suggests as association between prediabetes and complications of diabetes such early nephropathy(10%) , small fiber neuropathy(18-25 %), early retinopathy (8-12%) and risk of macrovascular disease (52%) . - Screening for prediabetes is designed to save lives or enhance an individual's quality of life by early detection so that screening will minimize the risk of developing diabetes or its complications .

NCT ID: NCT05863832 Recruiting - Clinical trials for Surgical Site Infections

Study to Assess the Safety & Efficacy of Oral Ciprodiazole Versus Currently Used Ciprofloxacin & Metronidazole

CIPRO-001
Start date: August 17, 2021
Phase: Phase 4
Study type: Interventional

This study aims to assess the safety & efficacy of Oral Ciprodiazole® versus currently used Ciprofloxacin Tablets & Metronidazole tablets in pelvi-abdominal infections and following IV antibiotics in post-operative period, for pelvi-abdominal surgeries or acute conditions

NCT ID: NCT05863546 Recruiting - Clinical trials for Carpal Tunnel Syndrome

Effect of Different Doses of US in the Treatment of CTS

Start date: September 10, 2023
Phase: N/A
Study type: Interventional

The purpose of this study will be to investigate the effective dose of therapeutic ultrasound in the treatment of carpal tunnel syndrome on pain level, functional ability, motor and sensory nerve conduction parameters and pinch strength.

NCT ID: NCT05863286 Recruiting - Clinical trials for Subluxation of Temporomandibular Joint

Assessment of Botulinum Toxin Injection for Treatment of Temporomandibular Joint Dislocation

Start date: December 30, 2022
Phase: N/A
Study type: Interventional

Assessment of the effect of Botulinum toxin injection on the frequency of luxation and TMJ Pain in patients with TMJ dislocation either chronic recurrent dislocation or subluxation

NCT ID: NCT05862298 Recruiting - Clinical trials for Intravascular Volume

Spinal-Induced Hypotension in Geriatric Patients

Start date: May 1, 2023
Phase:
Study type: Observational

The study will be conducted to asses preoperative condition of venous system by VExUS score and it's relation with the incidence of spinal induced hypotension in geriatric patients undergoing surgery with spinal anaesthesia.

NCT ID: NCT05861921 Recruiting - Missing Teeth Clinical Trials

Single-retainer Lithium Di-silicate Versus Zirconia Resin Bonded Bridge for Replacement of an Anterior Missing Tooth.

RBFPD
Start date: July 1, 2023
Phase: N/A
Study type: Interventional

First, Participants in this study will be recruit according to inclusion criteria. Proper examination for the participants (clinically and radiographically). Preparation for abutment tooth for Resin bonded fixed partial denture. Checking and verification for the restoration (trying). Clinical assessment and survival evaluation of the final restoration on delivery and on follow-up every 12 weeks for 12 months.