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NCT ID: NCT06276205 Recruiting - Dyslipidemias Clinical Trials

Vitamin D & Levothyroxine Combination Versus Levothyroxine on Lipid Profile in Hypothyroidism

ViDaLLiT
Start date: March 1, 2024
Phase: Phase 3
Study type: Interventional

The goal of this clinical trial is to study the improvement of lipid levels in hypothyroid individuals after staring treatment. The main question it aims to answer is: • whether adding Vitamin D to standard therapy has any additional benefits Participants will be given Vitamin D in replacement doses according to their pre-existing Vitamin D level in addition to levothyroxine. Researchers will compare them with another group receiving only levothyroxine to see how much lipids improve in them

NCT ID: NCT06275646 Completed - Hypospadias Clinical Trials

Comparison Of Outcome Of Different Layers in Hypospadias Surgery

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

To compare the outcome of applying autologous platelet-rich plasma membrane layer and dartos fascial flap versus only dartos fascial flap in mid and distal penile hypospadias surgery. A total of 220 patients fulfilling the selection criteria were admitted after taking informed consent. Cases were randomly divided into groups A and B using a random generator of the Excel program. In group A, dartos flap and PRP sheet layer were applied and in group B, only a preputial dartos fascial flap was applied

NCT ID: NCT06274216 Completed - Clinical trials for Osseointegration Failure of Dental Implant

The Effect of Vitamin D Supplementation on Dental Implant Osseointegration: A Randomized Controlled Trial

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

Dental implantation is a new technique for the single or more missing tooth replacement. Dental professionals might utilize the findings of this investigation to generate local data and learn more about how vitamin D affects bone metabolism and implant osseo-integration. The long-term success of dental implants would also be enhanced and preserved with the right medical use of vitamin D

NCT ID: NCT06273930 Recruiting - Sensitivity, Tooth Clinical Trials

Reduction of Dentine Hypersensitivity After Use of Different Dentifrices

Dentrifices
Start date: February 1, 2024
Phase: Phase 1
Study type: Interventional

To assess the impact of the use of 5% Calcium Sodium Phosphosilicate or 8% Arginine dentifrices on dentinal hypersensitivity following non-surgical periodontal therapy in patients with periodontitis.

NCT ID: NCT06271096 Completed - Seizures Clinical Trials

Intramuscular Midazolam Versus Intravenous Diazepam for Acute Seizure in Children

Start date: November 1, 2019
Phase: Early Phase 1
Study type: Interventional

IM-midazolam in acute seizures, whenever IV cannulation is not possible. It is easy to administer and can be used in prehospital settings as IV cannulation requires experience, especially in pediatric age group. Moreover, the transit time to the hospital can be prolonged in our areas which can delay the treatment if intravenous cannulation is considered. More studies are required to assess the feasibility of administering IM-midazolam in a prehospital setting to control acute seizures

NCT ID: NCT06267404 Recruiting - Back Pain Clinical Trials

Effectiveness of Iliopsoas Positional Release Versus Conventional Exercises in the Management of Sub-acute Back Pain.

Start date: February 21, 2024
Phase: N/A
Study type: Interventional

Recommended treatment for chronic non-specific LBP is exercise therapy, behavioral therapy including pain management, or a combination of these; There is not enough evidence to establish recommendations for which one is the most appropriate. The primary objective of this study is to explore the effects of Ilio-psoas Release on Sub-acute back pain, ROM & functional disability

NCT ID: NCT06267118 Recruiting - Clinical trials for Acute Bronchiolitis Due to Respiratory Syncytial Virus

Comparative Efficacy of Hypertonic Saline vs Adrenaline Nebulization in Acute Bronchiolitis

children
Start date: November 1, 2023
Phase: Phase 3
Study type: Interventional

The goal of this clinical trial is to compare the efficacy of hypertonic saline nebulization with adrenaline nebulization in the treatment of acute bronchiolitis in children. Main aim is to evaluate the following in both group of patients 1. Improvement in Wood-Downes clinical score (WDF score) in bronchiolitis 2. Length of Hospitalization

NCT ID: NCT06263335 Completed - Suicidal Ideation Clinical Trials

MBI for Psychological Distress, SI and NSSI Among Young Adults

Start date: February 28, 2022
Phase: N/A
Study type: Interventional

Designed to measure the impact of Mindfulness Based Intervention on depression, anxiety, stress, psychological distress, Suicidal Ideation, Non-Suicidal Self Injury urge and Mindfulness in young adults. Those individuals who agree to participate in the trial and identified with high levels of psychological distress and Suicidal Ideation, randomly divided into interventional (n=30) and control (n=30) groups. The Mindfulness Based Stress Reduction intervention then administered to the interventional group for eight weeks and pre and post intervention assessment done for both the groups.

NCT ID: NCT06260241 Recruiting - Concealed Penis Clinical Trials

Gain in Stretched Penile Length After Phalloplasty With & Without Penile Traction in Children.

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

The goal of this Randomized Controlled Trial is to assess the gain in stretched penile length after phalloplasty with & without penile traction in children of age group 4 to 13 years presenting in hospital with the complaint of concealed penis. The main question[s] it aims to answer is: • Gain in stretched penile length after phalloplasty with and without penile traction in children.

NCT ID: NCT06256302 Recruiting - Pain Clinical Trials

Transverses Abdominis Plane Block Versus Local Wound Infiltration in Total Abdominal Hysterectomy

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

To compare the transverses abdominis plane block outcome versus local wound infiltration for postoperative analgesia in patients undergoing total abdominal hysterectomy.