Clinical Trials Logo

Filter by:
  • Not yet recruiting  
  • Page [1] ·  Next »
NCT ID: NCT06445036 Not yet recruiting - Hypoparathyroidism Clinical Trials

Tunisian Clinical Registry on Hypoparathyroidism and Pseudo-hypoparathyroidism.

THYPARS
Start date: September 1, 2024
Phase:
Study type: Observational [Patient Registry]

Observational, multicenter, national, cross-sectional study aiming to describe the epidemiological clinical, biological and therapeutic profile of patients suffering from defect in secretion (hypoparathyroidism) or action (pseudo-hypoparathyroidism) of parathyroid hormone.

NCT ID: NCT06210672 Not yet recruiting - Clinical trials for Gamma-sarcoglycanopathy

Natural History Study in Patients With LGMDR5/2c

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

Prospective, longitudinal, interventional, multicenter natural history study to better understand the LGMDR5/2c disease physiopathology. The duration of participation for each patient will be up to 24 months.

NCT ID: NCT06190535 Not yet recruiting - Clinical trials for Postpancreatectomy Hemorrhage

Can Administration of Etamsylate Reduce Postpancreatectomy Hemorrhage

PGPPH1
Start date: January 1, 2024
Phase: N/A
Study type: Interventional

In several studies comparing the tow types of pancreato-digestive anastomosis: pancreatogastrostomy (PG) and pancreatojejunostomy (PJ), authors concluded that PG exposed to more postpancreatectomy hemorrhage (PPH) especially early, digestive and moderate hemorrhage classified as type A according to the classification of the ISGPS. In this way we try to test the ability of the enteral administration through the nasogastric tube of Etamsylate for 48 hours after Whipple to reduce the rate of digestive PPH and mortality.

NCT ID: NCT05621876 Not yet recruiting - Clinical trials for Primary Immunodeficiency Diseases

Evaluation of an IgG Deficiency Rapid Screening Test: A Performance Study With Primary Immunodeficiency (PID) Patients in Tunisia

Start date: May 15, 2024
Phase:
Study type: Observational

To evaluate the usability and utility of the device, % agreement between the PID-RDT and the referent assay (serum/plasma), and % agreement between capillary blood and venous blood samples using the PID-RDT within confirmed PID patients prior to receipt of their monthly IV-Ig treatment.

NCT ID: NCT04405921 Not yet recruiting - COVID-19 Clinical Trials

Hydroxychloroquine, Azithromycin in the Treatment of Covid-19

PACTT
Start date: July 2020
Phase: Phase 3
Study type: Interventional

This study investigates the efficay and tolerance of 5-days course of hydroxychloroquine or hydroxychloroquine and azithromycin of patients with COVID-19 infection. The investigators will undertake a randomized, double-blind, controlled Trial in the region of Sousse Tunisia

NCT ID: NCT04377646 Not yet recruiting - COVID19 Clinical Trials

A Study of Hydroxychloroquine and Zinc in the Prevention of COVID-19 Infection in Military Healthcare Workers

COVID-Milit
Start date: May 4, 2020
Phase: Phase 3
Study type: Interventional

A multicenter randomized clinical trial aiming to assess the efficacy of hydroxychloroquine associated to Zinc compared to hydroxychloroquine, in the prevention of Military Health Professionals Exposed to SARS CoV2 in Tunisia

NCT ID: NCT04361032 Not yet recruiting - COVID19 Clinical Trials

Assessment of Efficacy and Safety of Tocilizumab Compared to DefeROxamine, Associated With Standards Treatments in COVID-19 (+) Patients Hospitalized In Intensive Care in Tunisia

TRONCHER
Start date: September 4, 2020
Phase: Phase 3
Study type: Interventional

Assessment of Efficacy and Safety of Tocilizumab Compared to DefeROxamine, associated with standards treatments in COVID-19 (+) patients, Hospitalized In Intensive care in Tunisia. Multicentric, comparative, randomized study.

NCT ID: NCT04176770 Not yet recruiting - Post Operative Pain Clinical Trials

Comparaison of ESP Block and TAP Block

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

This study aim to compare the efficiency and the analgesic effect of Erector Spinal Plane Block versus TAP Block after laparoscopic cholecystectomy.

NCT ID: NCT03752931 Not yet recruiting - Clinical trials for Postoperative Cardiac Complication

Celiprolol Versus Ditiazem for the Prevention of Postoperative Cardiac Arrythmias in Thoracic Surgery

CelDilPreCA
Start date: December 2018
Phase: Phase 2
Study type: Interventional

Cardiac arrythmias are the most common cardiac complications after thoracic surgery. They are made primarily of postoperative atrial fibrillation (POAF). They are associated with an increased risk of stroke, increased length of hospital stay and cost of care, and increased long-term mortality. Randomized , single-blind prospective study in the anesthesia and intensive care department of Abderrahmen Mami hospital Ariana Tunisia comparing the efficacy of Diltiazem versus Celiprolol in the prevention of postoperative cardiac arrythmias in patients proposed for pneumonectomy and bilobectomy.

NCT ID: NCT02428868 Not yet recruiting - Anemia Clinical Trials

IV Iron in Association With Tranexamic Acid for Hip Fracture

Start date: April 2015
Phase: N/A
Study type: Interventional

It is a prospective randomized controlled study aiming to test if tranexamic acid combined to intravenous iron before and after surgery for hip fracture in elderly can decrease peri-operative red cell transfusion.