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NCT ID: NCT06469216 Recruiting - Clinical trials for Acute Radiation Enteritis

Efficacy of Hyaluronic Acid in Prevention of Acute Radiation Proctitis

Start date: April 1, 2024
Phase: Phase 1/Phase 2
Study type: Interventional

A randomized placebo-controlled clinical trial to evaluate efficacy of hyaluronic acid in prevention of acute radiation proctitis among oncology patient population especially who are diagnosed with abdomeno-pelvic tumors and subsequently required radiotherapy.

NCT ID: NCT06468904 Recruiting - Chronic Neck Pain Clinical Trials

Efficacy of Cervical Stabilization Exercises on Hand Grip Strength in Chronic Myofascial Neck Pain

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

The purpose of this study is to examine effect of cervical stabilization exercises on hand grip strength, key pinch strength, pain intensity, pain pressure threshold and hand function in chronic myofascial neck pain patients.

NCT ID: NCT06468891 Recruiting - Clinical trials for Stress Urinary Incontinence

Analyzing Gait Parameters Among Women With and Without Stress Urinary Incontinence

GPWSUI
Start date: June 16, 2024
Phase:
Study type: Observational

This study will contribute to the existing body of knowledge on stress urinary incontinence and its impact on gait. The findings may have implications for the development of targeted interventions and rehabilitation strategies to improve mobility and quality of life in women with stress urinary incontinence

NCT ID: NCT06467318 Recruiting - Clinical trials for Primary and Secondary Spontaneous Pneumothorax

Does Non-Steroidal Anti-inflammatory Drugs Decrease the Quality of Pleurodesis After Mechanical Pleural Abrasion/Pleurectomy for Treatment of Pneumothorax?

Start date: September 1, 2023
Phase: Phase 1/Phase 2
Study type: Interventional

Investigators aim to assess if NSAIDs affect the quality of pleurodesis resulting from mechanical pleurodesis (open surgery or VATS) regarding : Primary outcome: Recurrence of pneumothorax in 6 monthes. (assessed by X ray after 2 weeks and 6 months or symptoms requiring X ray at any timing) Secondary outcome: ▪ Adjusted Length of stay ( from day zero surgery day to discharge ). ▪ Time of removal of the chest Tube .(relatively longer with air leak presence). ▪ Need of opioids (N-SAID may decrease the need of opioids) .

NCT ID: NCT06467240 Not yet recruiting - Maxillary Anomaly Clinical Trials

Evaluation of the Hybrid Rapid Maxillary Expander Assisted With Micro-osteo Perforation (MOPs) in Adult.

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

This study will be directed for Evaluation of the hybrid rapid maxillary expander assisted with Micro-osteo perforation (MOPs) in adults

NCT ID: NCT06466954 Completed - Clinical trials for Primary Dysmenorrhea

Correlation Between Spinopelvic Alignment and Uterine Dimensions in Primary Dysmenorrhea

Start date: March 1, 2022
Phase:
Study type: Observational

This study was conducted to investigate the correlation between spinopelvic alignment and uterine dimensions in primary dysmenorrhea.

NCT ID: NCT06466538 Recruiting - Clinical trials for Microbial Colonization

Investigate"Clinically" the Effectiveness of Boswellia Based Intracanal Medication Compared to Calcium Hydroxide Ca(OH)2 and Ledermix on the Levels of Bacteria and Inflammatory Cytokines in Root Canals and Periradicular Tissues of Teeth With Apical Periodontitis

Start date: June 1, 2022
Phase: Phase 2/Phase 3
Study type: Interventional

The objective of this study is to investigate "clinically" the effectiveness of Boswellia based intracanal medication compared to the commonly used intracanal medicaments (calcium hydroxide Ca(OH)2 and Ledermix) on the levels of bacteria and inflammatory cytokines in root canals and periradicular tissues of teeth with apical periodontitis.

NCT ID: NCT06466421 Not yet recruiting - Hemodialysis Clinical Trials

Fexofenadine Versus Gabapentin for Uremic Pruritus in Patients on Regular Hemodialysis

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

Several studies investigated the effectiveness of Gabapentin in Uremic Pruritus (UP). No previous studies investigated the use of fexofenadine in UP. The aim of this trial is to assess the safety and possible efficacy of fexofenadine in patients with UP.

NCT ID: NCT06466369 Active, not recruiting - Clinical trials for BPH With Other Lower Urinary Tract Symptoms

Administration of Tadalafil in Patients With Benign Prostatic Hyperplasia

Start date: March 15, 2024
Phase: Phase 3
Study type: Interventional

The aim of the present study is to evaluate the efficacy and safety of once daily administration PDE5 inhibitors, tadalafil for 3 months as anti-inflammatory, antiproliferative and relaxant effects in ED with BPH patients.

NCT ID: NCT06466343 Recruiting - Cesarean Scar Niche Clinical Trials

Immunohistopathologic Findings of Cesarean Scar Niche

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

Niche is iatrogenic pouch like defect, present on the uterine isthmus' anterior wall where a previous caesarean section scar was made. Still, a niche has generally been defined as the myometrium's depression of at least 2 mm (Lumbanraja et al., 2024). The literature is lacking in information about the accurate histopathologic characteristics of cesarean scar niche ridges that have been removed by hysteroscopy, as well as what critical findings to highlight and what gynaecologists can anticipate from pathology reports of cesarean scar niche specimens (AbdullGaffar & Almulla ,2022). In this study the aim of the work is to study the histopathologic findings in cesarean scar niche specimens repaired by hysteroscopy in our institution, identify the causes of local thinning of the uterine scar after c-section to direct gynecologists regarding the efficacy of their hysteroscopic corrective repair of cesarean scar niche concerning the amelioration of symptoms, restoration of fertility, and patient follow-up.