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NCT ID: NCT02736058 Recruiting - Adherent Placenta Clinical Trials

Surgical Classification of Abnormal Placentation

Start date: February 2016
Phase: N/A
Study type: Interventional

Reaching the proper pre-operative diagnosis for abnormal placentation in crucial to markedly decrease the intra-operative complications as well as the maternal morbidity and mortality. In this trial researchers aim to set up some pre-operative sonographic criteria that would help in planning the surgical procedure as well as setting up a surgical classification for the abnormally adherent placenta.

NCT ID: NCT02736019 Recruiting - Hysteroscopy Clinical Trials

Tramadol Versus Celecoxib for Reducing Pain During Office Hysteroscopy in Post Menopausal Women

Start date: June 2016
Phase: Phase 3
Study type: Interventional

Two hundreds and twenty five postmenopausal women undergoing outpatient hysteroscopy and endometrial biopsy will be randomly divided into three equal groups. To ensure blinding the investigators will use the double dummy technique in which group 1 will receive Tramadol 100mg (Trama®, Global Napi, Giza, Egypt) orally in addition to a placebo similar to Celecoxib, group 2 will receive Celecoxib 200mg (Celebrex® 200, Pfizer, USA) in addition to a placebo similar to Tramadol, and group 3 will received a placebo similar to Tramadol and a placebo similar to Celecoxib. All drugs will be given 2 hours before the procedure. An independent person will generate the allocation sequence using computer generated random numbers. Patient's perception of pain will be assessed for each group during the procedure, immediately after and 30 min after the procedure with the use of visual analogue scale (VAS).

NCT ID: NCT02735655 Recruiting - Clinical trials for Gastrointestinal Endoscopy Training

Global State of Digestive Endoscopy Training Survey

Start date: April 2016
Phase: N/A
Study type: Observational

This is a 10 minutes web based survey aims at exploring the current, global state of digestive endoscopy training among physicians to identify what are the unmet needs and how to improve it.

NCT ID: NCT02733952 Recruiting - Clinical trials for Post Operative Hemorrhage

Intravenous Tranexamic Acid Versus Pericervical Tourniquet To Decrease Blood Loss In Trans-Abdominal Myomectomy

Start date: August 2015
Phase: Phase 3
Study type: Interventional

Intravenous Tranexamic Acid Versus Pericervical Tourniquet To Decrease Blood Loss In Trans-Abdominal Myomectomy

NCT ID: NCT02727946 Recruiting - Multiple Trauma Clinical Trials

Tissue Perfusion Indices as Predictor of Outcome in Poly Trauma Patients

Start date: May 2016
Phase: N/A
Study type: Interventional

Early intervention and resuscitation based upon a lot of clinical, laboratory findings make a big difference regarding outcome in poly trauma patients, the study uses the dynamic lactate change and the difference between arterial and venous CO2, oxygen tension or content as indicators for tissue perfusion.

NCT ID: NCT02723461 Recruiting - Clinical trials for Failed Induction (of Labor) by Oxytocin

Continuous Oxytocin Infusion Versus Pulsatile Intravenous Oxytocin for Augmentation of First Stage of Labor

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

Comparing continuous intravenous oxytocin infusion with pulsatile administration of intravenous oxytocin for augmentation of the first stage of labor.

NCT ID: NCT02714725 Recruiting - Clinical trials for Sublingual Microcirculation

Effect Of Dexmedetomidine On Sublingual Microcirculation In Patients Undergoing On Pump CABG Surgery

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

This study is designed to explore the possible effects of dexmedetomidine infusion on sublingual microcirculation in patients undergoing on-pump coronary artery bypass graft surgery

NCT ID: NCT02704611 Recruiting - Fibromyalgia Clinical Trials

Direct Current Stimulation for Treatment of Fibromyalgia

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

The aim of this study is to assess the effectiveness of transcranial direct current stimulation (tDCS) in treating fibromyalgia. Participants will be randomly assigned to one of the two groups: Group I (Intervention group) tDCS (2mA for 25 minutes on 5 consecutive days/week for 2 weeks with the anode centered over M1 bilaterally Anodal tDCS for 20 minutes at 1.5 mA (15 s ramp in and 15 s ramp out) will be applied daily for 10 consecutive days (5 sessions/week) . The anodal electrode (24 cm² with current density of 0.08 mA (2mA/24 cm²) will be placed over the left primary motor area in group I, and the reference electrode (24 cm² will be fixed over the contralateral arm (extracephalic). Daily tDCS was given to prolong and stabilize these long-lasting after-effects. Group II will receive sham tDCS will be applied using the above described parameters in group I. For sham tDCS, the placement of the electrodes, current intensity, and ramp time was identical to real tDCS stimulation group; however, the stimulation lasted only for 30 Sec. However, since none of the patients have been experienced tDCS previously, they were unaware of which stimulation is real and which sham is. The investigator responsible for delivering tDCS had no contact with the patients. All study participants will be followed up by the same evaluation sheet and by an evaluator who are blinded to the type of intervention she /he has received.Evaluation will be done pre assessment, post 5 sessions, post 10 sessions, post one month and post 2 months by using wide spread pain index (WPI) & symptoms severity of fibromyalgia, measuring visual analogue scale (VAS), Depression and anxiety will be assessed using Hamilton Depression Scale (HDS) and anxiety scale, pain sensitivity threshold by using Electronic Von Frey unit EVF4 . Determination of human beta-endorphin level before start sessions and after end 10 sessions.

NCT ID: NCT02702674 Recruiting - Poor; Labor Clinical Trials

The Effect of Coadministration of Oral Propranolol to Oxytocin on Induction of Labor

Start date: December 2015
Phase: Phase 3
Study type: Interventional

The effect of coadministration of oral propranolol to oxytocin on induction of labor.

NCT ID: NCT02698644 Recruiting - Clinical trials for Fallopian Tube Occlusion

Hysteroscopic Tubal Occlusion With the Use of Iso Amyl-2-cyanoacrylate

Start date: January 2016
Phase: Phase 1
Study type: Interventional

Is to assess the effectiveness of hysteroscopic tubal application of Iso Amyl-2-cyanoacrylate in occluding uterine tubes of women, which would make it an easy approach for occluding tubes with hydrosalpinx prior to IVF and in tubal sterilization.