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Hypotension clinical trials

View clinical trials related to Hypotension.

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NCT ID: NCT02001298 Completed - Clinical trials for Hypotension, Controlled

Remifentanil and Nitroprusside for Controlled Hypotension

Start date: June 2012
Phase: N/A
Study type: Interventional

The purpose of this study is the comparison of the cardiovascular effects of remifentanil and nitroprusside for controlled hypotension

NCT ID: NCT01994785 Recruiting - Hypotension Clinical Trials

Use of Capnography in EGD and Colonoscopy With Moderate Sedation.

Start date: November 2013
Phase: N/A
Study type: Interventional

This study will provide capnography monitoring during routine upper endoscopy and colonoscopy with moderate sedation in order to see if it improves safety.

NCT ID: NCT01988181 Completed - Clinical trials for End Stage Renal Failure on Dialysis

Adjusting Fluid Removal Based on Blood Volume in Hemodialysis: A Randomized Study

Start date: June 2014
Phase: N/A
Study type: Interventional

As kidney function declines, the ability to maintain water balance is impaired and is most often treated with hemodialysis. The removal of excess water in hemodialysis often leads to a sudden drop of blood pressure and causes symptoms of dizziness, light-headedness, cramping, and chest pain. This sudden drop in blood pressure has been linked with complications of heart attacks, strokes and even death. Research has focused on different ways to prevent dangerous drops in blood pressure during hemodialysis. One way is the use of blood volume monitoring biofeedback technology to monitor the patient's relative blood volume and automatically reduce the amount of fluid that is being removed when the blood volume is low to prevent the drop in blood pressure from occurring. This type of biofeedback device is currently available on some hemodialysis machines and while this approach appealing, it is not clear how effective this form of biofeedback is in preventing the drops in blood pressure. We plan to determine if the use of biofeedback based on the changes in the patient's blood volume will reduce the number of sudden drops in blood pressure that occur during hemodialysis. To do this, we will compare patients treated with this technology to current hemodialysis practices and follow them for important adverse outcomes. The result of interest will be the frequency of hemodialysis sessions complicated by a sudden symptomatic drop in blood pressure. We also plan to monitor the amount of water in the different body compartments, blood pressure, blood pressure medication use, markers of heart function, and patient symptoms and quality of life. We hope that by providing information on this technology we can reduce the sudden drops in blood pressure in hemodialysis, the associated rates of serious disease or death, and improve patient quality of life.

NCT ID: NCT01971008 Completed - Parkinson's Disease Clinical Trials

Abdominal Binder to Treat Orthostatic Hypotension (OH) in Parkinson's Disease (PD)

ABOHP
Start date: May 2013
Phase: Phase 2
Study type: Interventional

The purpose of the present study is to determine whether the use of an abdominal binder is effective in the non-pharmacological management of orthostatic hypotension in patients suffering from Parkinson's disease

NCT ID: NCT01967914 Completed - Clinical trials for Spinal Induced Hypotension

PVI for Prediction of Spinal Induced Hypotension

Start date: October 2013
Phase: N/A
Study type: Observational

The hypothesis is that plethysmography variability index can predict the occurrence of hypotension after spinal anesthesia for cesarean delivery

NCT ID: NCT01956981 Completed - Hemorrhage Clinical Trials

Controlled Hypotension During Functional Endoscopic Sinus Surgery

Start date: January 2012
Phase: Phase 4
Study type: Interventional

It is very important to decrease the bleeding during functional endoscopic sinus surgery (FESS) in order to increase the visibility of the surgical site. Our primary goal was to investigate the effects of magnesium sulfate and dexmedetomidine used for controlled hypotension on visibility of surgical site.

NCT ID: NCT01954446 Withdrawn - Healthy Clinical Trials

A Novel Non-interfering Arterial Blood Pressure Monitoring Device

Start date: April 2013
Phase: N/A
Study type: Interventional

The primary purpose of this investigation is to validate the performance and safety of the Investigational Device (ID) against a validated and legally cleared device for measuring Blood Pressure (BP). The secondary purpose is to validate the performance of the ID over a period of 24 hours against a validated and legally cleared device for Ambulatory Blood Pressure Monitoring (ABPM).

NCT ID: NCT01951079 Not yet recruiting - Hypotension Clinical Trials

Intra Amniotic Injection of DIGOXIN for Feticide in Second Trimester Termination of Pregnancy

Start date: November 2013
Phase: Phase 3
Study type: Interventional

In second trimester abortion above 22 weeks the investigators usually inject intra-cardiac Kcl for feticide. Digoxin intra-amniotic injection has been described in the literature in doses of 1-1.5 mg. with a success rate of about 80%, and up to 24 weeks. Our aim in this study is to investigate the safety and success rate of 1.5-2 mg. digoxin, intra-amniotic up to 30 weeks pregnancy .

NCT ID: NCT01941472 Not yet recruiting - Hypotension Clinical Trials

Transcutaneous pO2, Transcutaneous pCO2 and Central Venous pO2 Variations to Predict Fluid Responsiveness

Start date: September 2013
Phase: N/A
Study type: Interventional

Fluid challenge is often carried out in critical ill patients. Its responsiveness usually requires invasive monitoring. To use non-invasive methods is very tempting. We hypothesize that transcutaneous pO2,transcutaneous pCO2 and Central Venous pO2 variations provide feasible estimation on fluid responsiveness in critical ill patients.

NCT ID: NCT01930227 Completed - Hypotension Clinical Trials

Transcutaneous Electrical Acupoint Stimulation(TEAS) for Hypotension After Spinal Anesthesia in Parturients

THSAP
Start date: September 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effect of TEAS on hypotension after spinal anesthesia in patients undergoing cesarean section