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NCT ID: NCT03135301 Recruiting - Infertility, Female Clinical Trials

Letrozole in Clomiphene Resistant Infertile Women With Polycystic Ovarian Syndrome

Start date: June 20, 2017
Phase: Phase 3
Study type: Interventional

Polycystic ovary syndrome accounts for the vast majority of anovulatory symptoms and hyperandrogenism in women. The diagnosis of Polycystic ovary syndrome has life-long implications, with increased risk for infertility, metabolic syndrome, and type 2 diabetes mellitus, and possibly for cardiovascular disease and endometrial carcinoma. Polycystic ovary syndrome is diagnosed in adolescents with otherwise unexplained, persistent hyperandrogenic anovulatory symptoms that are inappropriate for age and stage of adolescence. It should be considered in any adolescent girl with a chief complaint of hirsutism, treatment-resistant acne, menstrual irregularity, acanthosis nigricans, and/or obesity

NCT ID: NCT03133975 Recruiting - Dyslipidemias Clinical Trials

Vitamin D Supplementation for Treatment of Dyslipidemia

Start date: April 1, 2017
Phase: Phase 3
Study type: Interventional

This study will be conducted to Assess possible reduction in lipid profile (LDL-Triglecerides-cholesterol) among pre-menopausal women in vit D group compared to standard treatment group after 3 months & 6 month of follow up as prophylaxis step for atherosclerosis.

NCT ID: NCT03129022 Recruiting - Vaginal Delivery Clinical Trials

Failed Epidural Anesthesia During Labor: Evaluation of Risk Factors and Outcome

Start date: April 30, 2017
Phase: N/A
Study type: Interventional

Women requesting epidural analgesia will receive a bolus of intravenous infusion of lactated Ringer's solution before initiation of the procedure. An 18-gauge Tuohy needle and closed-tip clear catheter with three lateral orifices (Portex, Smith Medical, Hythe, UK) were used in the sitting or lateral position, with a loss-of-resistance to air technique. Epidural catheters will be inserted 5-6 cm inside the epidural space. A test dose of 2 ml of lidocaine 2% iss initiated followed by a loading dose of 10 ml of bupivacaine 0.25%. Analgesia is established and maintained throughout labor and delivery using 0.125% bupivacaine with fentanyl 2 μg/ml with patient-controlled epidural analgesia by means of a continuous epidural infusion (8 ml/h basal rate) and patient-controlled boluses (3 ml each) with 20-minlock-out intervals, continued at the same bolus dose until delivery. Pain was evaluated using a 0-10 cm visual analogue scale (VAS) before, 15 and 30 min after the loading dose followed by hourly assessment until delivery. VAS score assessment was based specifically on abdominal or back pain resulting from contractions

NCT ID: NCT03126838 Recruiting - Diaphragm Disease Clinical Trials

Diaphragmatic Dysfunction and Cardiac Surgery; Perioperative Assessment and Effect on Outcome

Start date: March 1, 2017
Phase: N/A
Study type: Observational

This study evaluates incidence of diaphragmatic dysfunction after cardiac surgery and its effect on outcome of surgery.

NCT ID: NCT03124472 Recruiting - Placenta Previa Clinical Trials

Effect of Uterine Artery Ligation Prior to Uterine Incision in Women With Placenta Previa

Start date: June 1, 2017
Phase: N/A
Study type: Interventional

Pfannenstiel incision of skin and opening of the anterior abdominal wall in layers. - The loose peritoneum of the lower uterine segment is dissected downwards to mobilize the urinary bladder and expose the lower uterine segment. - Uterine artery ligation was performed by grasping the broad ligament with thumb anterior and the index finger lifting the base below the site uterine incision; the uterine artery was singly ligated with No. 1 vicryl suture. Myometrium was included so that uterine vessels are not damaged. - Cresenteric lower uterine segment incision was performed as usual. Higher incisions were performed in cases where the traditional incision was expected to be directly through the placenta Delivery of the baby and placenta. - Closure of the uterine incision in 2 layers with N0. 1 vicryl suture. - Closure of the anterior abdominal wall in layers

NCT ID: NCT03123237 Recruiting - Hypertension Clinical Trials

Quantitative Renal Uptake Using TC99m DMSA in Hypertensive &/or Diabetic Patients.

Start date: July 2016
Phase: Phase 4
Study type: Interventional

the investigators explore the possible role of DMSA to detect renal affection in diabetic &/or hypertensive patients by detecting difference in counts using Tc 99m DMSA in control & diabetic &/or hypertensive patients.

NCT ID: NCT03122756 Recruiting - Cesarean Section Clinical Trials

Effect of Intravenous Dexamethasone Before Spinal Anesthesia on Post-cesarean Section Pain

Start date: August 1, 2017
Phase: Early Phase 1
Study type: Interventional

*Aim of the Work This study aims to assess the efficacy of intravenous injection of dexamethasone prior to spinal anesthesia in reducing post-cesarean section pain in women undergoing cesarean section.

NCT ID: NCT03121768 Recruiting - Bladder Cancer Clinical Trials

A New Prognostic Model for Predicting the Outcome of Patients With Non-muscle Invasive Bladder Cancer (NMIBC)

Start date: May 15, 2017
Phase: N/A
Study type: Observational

A prospective observational study to re-establish a new prognostic model for predicting the outcome in patients with non-muscle invasive bladder cancer (NMIBC) using the current recommendation regimen for intermediate and high risk groups and including all potential and highly prognostic factors.

NCT ID: NCT03116867 Recruiting - Clinical trials for Fallopian Tube Occlusion

Sonosalpingography After Hysteroscopic Tubal Occlusion

Start date: May 2017
Phase: N/A
Study type: Observational

Sonosalpingography is done to assess the efficacy of hysteroscopic tubal occlusion by roller ball electrode.

NCT ID: NCT03112135 Recruiting - Clinical trials for Intraoperative Bleeding

Effect of Topical and Systemic Tranexemic Acid on Bleeding During Ear Exploration Surgery

Start date: April 2017
Phase: Phase 2
Study type: Interventional

The effect of tranexamic acid (TXA) on bleeding and improvement of surgical field during ear exploration surgery is not clear yet. This study will conducted to answer this question.