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NCT ID: NCT06376019 Not yet recruiting - Edentulous Jaw Clinical Trials

Occlusion and Disocclusion Time in Immediately Loaded Overdentures Supported by Two Splinted Versus Non Splinted Interforaminal Implants

Start date: April 25, 2024
Phase: N/A
Study type: Interventional

complete denture wearers struggle to eat well with their dentures due to poor denture retention, stability, and occlusal disharmony. So, the current study protocol aims to compare the occlusion/ disocclusion time in immediately loaded implant retained overdentures supported by two interforaminal implants; splinted versus non splinted dental implants compared to the conventional complete denture.

NCT ID: NCT06374784 Not yet recruiting - Alveolar Bone Loss Clinical Trials

Autogenous Demineralized Dentin Graft Combined With Injectable PRF + Metronidazole Versus Autogenous Demineralized Dentin Graft Combined With Injectable PRF Versus Autogenous Demineralized Dentin Graft Alone for Alveolar Ridge Preservation

Start date: April 20, 2024
Phase: N/A
Study type: Interventional

The aim of this trial is to compare the effect of autogenous demineralized dentin graft combined with injectable PRF loaded with metronidazole (sticky demineralized tooth releasing metronidazole) versus autogenous demineralized dentin graft combined with injectable PRF (sticky demineralized tooth) versus autogenous demineralized dentin graft (ADDG) alone on alveolar ridge preservation after extraction of non restorable, infected single-rooted teeth

NCT ID: NCT06374771 Not yet recruiting - Postoperative Pain Clinical Trials

Analgesic Effect of Melatonin and Vitamin C Administration, Alone or In Combination in Major Abdominal Surgery.

Start date: April 27, 2024
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to compare the analgesic effect of melatonin, and vitamin C and their combination in patients aged 18-60 years old who will undergo major abdominal surgery with mid-line incision within an expected time of surgery from 3 to 5 hours e.g. radical cystectomy, radical prostatectomy, colectomy, sigmoidectomy, splenectomy, and CBD exploration through mid-line incision. This study hypothesizes that using both vitamin C and melatonin together as adjuvants will cause: - More reduction in total morphine consumption in the first 24 hours postoperatively - More reduction of the incidence of chronic post-surgical pain, than using each adjuvant alone. Participants will be allocated into three equal groups: Melatonin (M group) and vitamin C (V group), and Melatonin and vitamin C (VM group). Two hours before surgery all patients will receive the study drugs orally and will be continued for 3 days postoperative at the same time of the first administration; 10mg of melatonin for M group (Melatonin 10 mg - Puritan's Pride premium company), 1gm of vitamin C for V group (Sanso C 1000 mg - AUG pharma company), and 10mg of melatonin and 1gm of vitamin C for VM group. Researchers will compare: - The effect of melatonin, vitamin C, and their combination on postoperative opioid consumption - The severity of postoperative pain, using the Numerical Rating Scale (NRS) - Patients' satisfaction with a three-point scale - The time of the first requirement for rescue analgesia - The effect on the incidence of chronic post-surgical pain.

NCT ID: NCT06370221 Not yet recruiting - Psoriatic Arthritis Clinical Trials

The Effect of Psoriatic Arthritis on Female Sexual Dysfunction

Start date: June 1, 2024
Phase:
Study type: Observational

Psoriasis is one of the most common immunemediated chronic inflammatory skin disorders.

NCT ID: NCT06370156 Not yet recruiting - Plaque Psoriasis Clinical Trials

Evaluation of TWEAK in Plaque Psoriasis and Psoriatic Arthritis Patients

Start date: June 1, 2024
Phase:
Study type: Observational

Psoriasis vulgaris is associated with significant comorbidity including depression, increased risk of cardiovascular events, diminished quality of life, as well as overall increased mortality. Moreover, concomitant psoriatic arthritis is present in up to 40% of psoriasis patients or will develop in the future. To enhance quality of life and potentially lower the risk of concomitant disease in psoriasis patients, effective treatment of this immune-mediated systemic inflammatory disease is required

NCT ID: NCT06370078 Not yet recruiting - Septic Shock Clinical Trials

Effect of Early Administration of Albumin 20% Versus Crystalloid

Start date: May 1, 2024
Phase: N/A
Study type: Interventional

Sepsis and septic shock are global health problems, leading to a high mortality rate. They are often associated with extremely low blood pressure and multiple organ dysfunctions, which are the main causes of death in critically ill patients. Fluid resuscitation is one of the most critical treatments for patients with sepsis and septic shock. An early administration of an appropriate fluid to patients is considered the most effective way to increase blood pressure, improve tissue perfusion, and save their lives. Crystalloid fluids are a subset of intravenous solutions composed of mineral salts and other small, water-soluble molecules, including normal, isotonic or hypertonic saline, and various buffered solutions.

NCT ID: NCT06366737 Not yet recruiting - Clinical trials for Maxillary Prognathism

En-mass Retraction by Lingual Retractor Versus Clear Aligner Appliances

Start date: April 2024
Phase: N/A
Study type: Interventional

en-mass retraction by lingual retractor versus clear alighner therapy

NCT ID: NCT06363578 Not yet recruiting - Dexmedetomidine Clinical Trials

Different Doses of Dexmedetomidine in External Oblique Intercostal Plane Block in Splenectomy

Start date: April 20, 2024
Phase: N/A
Study type: Interventional

The aim of this study is to compare the analgesic effects of different doses of dexmedetomidine as an adjuvant in external oblique intercostal plane block (EOIPB) in splenectomy.

NCT ID: NCT06362005 Not yet recruiting - Lichen Planus, Oral Clinical Trials

The Efficacy of Selenium as an Alternative or Complementary Topical Treatment of Oral Lichen Planus

RCT
Start date: July 1, 2024
Phase: Phase 4
Study type: Interventional

evaluate clinically and biochemically the efficacy of topically applied selenium as complementary or alternative to triamcinolone acetonide 0.1% and tacrolimus 0.1% in patients with oral lichen planus.

NCT ID: NCT06359093 Not yet recruiting - Clinical trials for Non-carious Cervical Lesions

Prevalence Of Non-Carious Cervical Lesions, Associated Risk Indicators and Salivary Assessment Among Middle Adulthood Patients.

Start date: September 2024
Phase:
Study type: Observational

The aim of this study is to describe the prevalence of non-carious cervical lesions in middle adulthood patients attending the Cairo University Dental Educational Hospital and to analyze the distribution of lesions by gender and age, tooth functional group, jaw, arch side and tooth surface. Moreover, to explore the associated risk indicators of the lesions as well as the quantity of saliva, as one of the potential etiological factors, will be assessed.