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NCT ID: NCT06452563 Active, not recruiting - Malnutrition Clinical Trials

Amino Acids Supplementation and Exercise Intervention in Hemodialysis Patients

Start date: May 12, 2024
Phase: Phase 4
Study type: Interventional

The goal of this randomized clinical trial is to observe the effect of Amino acids (AAs)supplementation and exercises in haemodialysis patients . The main question it aims to answer is : Does AAs supplementation and regular exercises have an effect on the muscle mass and function in haemodialysis patients ? Participants will receive daily a total of six tablets of amino acids supplementation divided into three doses. And some Participants will also be asked to do intradialytic exercise. Researchers will compare the effects of these interventions on the muscle mass and fatigue, among four groups: 1. A group that will be only taking AAs supplementation 2. A group taking AAs supplementation along with intradialytic exercise 3. A group only performing intradialytic exercise 4. A passive control group This will be monitored through BMI, anthropometric measures, Musculoskeletal ultrasound assessment of the quadriceps muscle , fatigue questionnaires and sit and stand test.

NCT ID: NCT06452511 Not yet recruiting - PCOS Clinical Trials

Comparing the Effect of Metformin vs. Pep2dia as an Adjunct to Letrozole on Ovulation Induction and Pregnancy Outcomes in Overweight Women With PCOS

Start date: July 1, 2024
Phase: Early Phase 1
Study type: Interventional

The goal of this clinical trial is to compare the effects of Metformin versus Pep2dia as adjunct treatments to Letrozole on ovulation induction and pregnancy outcomes in overweight women with polycystic ovary syndrome (PCOS). The main questions it aims to answer are: Does Metformin improve ovulation rates more effectively than Pep2dia when used alongside Letrozole? Does Pep2dia enhance pregnancy outcomes compared to Metformin in this patient population? Participants will: Receive either Metformin or Pep2dia in addition to Letrozole. Undergo regular monitoring for ovulation and pregnancy outcomes. Researchers will compare the Metformin group to the Pep2dia group to see if there is a significant difference in ovulation and pregnancy rates between the two treatments.

NCT ID: NCT06452368 Completed - Clinical trials for Class III Malocclusion

Palatal Versus Buccal Protraction Using Plates Assisted With Facemask in Growing Class III Patients

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

to compare Palatal and buccal protraction using plates assisted with facemask in growing class III patients

NCT ID: NCT06452238 Recruiting - Clinical trials for Postoperative Analgesia

External Oblique Intercostal Plane Block Versus Transversus Abdominis Plane Block for Postoperative Analgesia in Adult Patients Undergoing Open Nephrectomy

Start date: June 12, 2024
Phase: N/A
Study type: Interventional

The aim of this study is to compare external oblique intercostal plane (EOIP) block and ultrasound guided transversus abdominis plane (TAP) Block for postoperative analgesia in adult patients undergoing open nephrectomy.

NCT ID: NCT06452225 Recruiting - Pediatrics Clinical Trials

Transversus Abdominis Plane Block Versus External Oblique Intercostal Plane Block for Postoperative Analgesia in Pediatrics Undergoing Open Nephrectomy

Start date: June 12, 2024
Phase: N/A
Study type: Interventional

The aim of this study is to compare the ultrasound guided TAP Block and EOIP block for postoperative analgesia in pediatrics undergoing open nephrectomy.

NCT ID: NCT06451900 Completed - Neonatal Jaundice Clinical Trials

Role of Fenofibrate in Neonatal Jaundice

Start date: July 1, 2023
Phase: Phase 4
Study type: Interventional

Fenofibrate appears to be an effective and safe drug for the treatment of neonatal hyperbilirubinemia. It has been proven that it decreases the duration of phototherapy and thus shortens the length of hospital stay. This study was performed to study the prophylactic role of fenofibrate in prevention of neonatal jaundice.

NCT ID: NCT06451406 Completed - Hyaluronic Acid Clinical Trials

Hyaluronic Acid Injection in the Glans Penis Versus Selective Serotonin Reuptake Inhibitors for Lifelong Premature

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

The aim of this study was to compare the effectiveness and safety of selective serotonin reuptake inhibitors (dapoxetine) and hyaluronic acid gel injection in the glans penis for lifelong premature.

NCT ID: NCT06451354 Recruiting - Cesarean Section Clinical Trials

Postoperative Analgesia After Cesarean Section; Comparison Among Ultrasound Guided Erector Spinae, Quadratus Lumborum or Transversus Abdominis Plane Blocks

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

The aim of this prospective randomized controlled study is to compare the analgesic efficacy of the ultrasound-guided erector spinae plane block, ultrasound-guided quadratus lumborum plane block, and ultrasound-guided transversus abdominis plane block in patients undergoing elective cesarean section.

NCT ID: NCT06451276 Not yet recruiting - Clinical trials for Cleft Lip and Palate

The Effectiveness of Adhesive Versus Conventional Nasoalveolar Molding on Children With Unilateral Cleft Lip and Palate

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

The present study will compare the effectiveness of adhesive nasoalveolar molding (GS-NAM) and conventional nasoalveolar molding on the alveolar ridge, nasal, and labial growth in children with unilateral cleft lip and palate. objectives: - 1. Evaluation of the anatomical position of the greater and lesser segments of the maxilla related to a stable midline anatomical point. 2. Evaluation of the nasal symmetry.

NCT ID: NCT06451237 Completed - Acne Vulgaris Clinical Trials

Acne Remission Maintenance by Weekend Systemic Isotretinoin

Start date: January 20, 2018
Phase: Phase 3
Study type: Interventional

The goal of this study is to learn if isotretinoin oral tablets as a weekend regimen are safe and effective to maintain freedom from acne lesions in young adults who have completed a full course of isotretinoin on daily basis and achieved total control of the acne activity.