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Postoperative clinical trials

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NCT ID: NCT02543580 Completed - Chronic Pain Clinical Trials

TEAS-induced Analgesia: Dual vs Single Acupoints

TADS
Start date: July 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effects of transcutaneous electric acupoint stimulation(TEAS) at single acupoint or dual acupoints on opioid consumption and postoperative pain in patients undergoing radical mastectomy

NCT ID: NCT01725464 Completed - Hypoxia Clinical Trials

The Effect of Nasal Cannula During the First 2 Hours Postoperative in Patient Undergoing Thoracotomy

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

During early postoperative after lung resection surgery, patients without oxygen supplementation may experience hypoxemia. Oxygen supplementation can be given via oxygen mask or cannular. In this study the investigators want to the sudy the effect of oxygen supplementation via oxygen cannular during the first 120 minutes after surgery

NCT ID: NCT01454609 Completed - Pain Clinical Trials

Safety and Efficacy of Bilateral Superficial Cervical Plexus Block in Thyroidectomy

Start date: January 2009
Phase: Phase 2
Study type: Interventional

With thyroid surgery being performed as an ambulatory procedure, most recent studies concerning post thyroidectomy analgesia are focused on regional techniques such as bilateral superficial cervical plexus block (BSCPB) and bilateral combined superficial and deep cervical plexus block. But, data regarding the efficacy of BSCPB are controversial. Hence the investigators compared the efficacy of BSCPB with 0.25% bupivacaine with or without clonidine in thyroidectomy, as preemptive analgesia. The hypothesis was bupivacaine with the addition of clonidine would help in reducing postoperative pain and thereby reduce the need for postoperative analgesia.

NCT ID: NCT01140529 Terminated - Delirium Clinical Trials

Dexmedetomidine for the Treatment of Delirium After Heart Surgery

DexinDelir
Start date: May 2010
Phase: Phase 3
Study type: Interventional

Primary hypothesis: Dexmedetomidine is equal or superior to haloperidol and placebo in the treatment of psychomotor confusion in patients who are recovering from heart surgery. Study design: Multi-centre, prospective, randomised, placebo-controlled double-blind study of dexmedetomidine vs. haloperidol for treatment of psychomotor confusion after cardiac surgery. Data will be analyzed in two steps: The primary comparison is between placebo and dexmedetomidine. If the effect of dexmedetomidine is significant, a secondary comparison between dexmedetomidine and haloperidol will follow.

NCT ID: NCT01139424 Not yet recruiting - Postoperative Clinical Trials

Closure of Anastomotic Leaks in the Stomach and Esophagus by Endoscopic Suturing

GASTROSUTURE
Start date: June 2010
Phase: N/A
Study type: Interventional

Patients with suspected leakage at the specified surgical anastomoses undergo an immediate diagnostic endoscopy as part of current clinical routine. Consenting patients meeting the inclusion criteria will undergo closure of the defect by endoscopic suturing in addition to standard surgical care.

NCT ID: NCT00864695 Completed - Anesthesia Clinical Trials

Role of Anesthesiologist-Patient Relationship

Start date: May 2007
Phase: N/A
Study type: Observational

Descriptive analytic survey of 1137 and 518 patients aged 16 years or more before and after anesthesia exposure, respectively to assess the anesthesiologist-patient relationship role on patient postoperative perception of the binominal anesthesia-anesthesiologist. The aim of this study was to assess the anesthesiologist-patient relationship role on patient postoperative perception of the binominal anesthesia-anesthesiologist. Period: may/2007 to may/2008

NCT ID: NCT00614588 Completed - Surgery Clinical Trials

Temperature Measurement in Post-Anesthesia Care Units

Start date: January 2008
Phase: N/A
Study type: Observational

This study will evaluate the accuracy of several thermometers and temperature changes during surgery and immediately after surgery.

NCT ID: NCT00478023 Completed - Hysterectomy Clinical Trials

A Study to Evaluate the Efficacy and Safety of Tapentadol (CG5503) in the Treatment of Acute Pain After Abdominal Hysterectomy

Start date: May 2007
Phase: Phase 3
Study type: Interventional

The main objective of this study is to demonstrate the efficacy and safety of multiple-dose application of three different oral doses of CG5503 IR (tapentadol immediate release) compared to placebo in women undergoing abdominal hysterectomy.

NCT ID: NCT00451373 Recruiting - Sepsis Clinical Trials

Acute Renal Failure in the Surgical Intense Care Units - NTUH-SICU-ARF (NSARF) Study

Start date: July 2006
Phase: N/A
Study type: Interventional

We examine the prognosis and etiology of postoperative acute renal failure

NCT ID: NCT00438035 Completed - Pain Clinical Trials

Heart Rate Variability and Postoperative Pain

ECG-Spectral
Start date: February 2007
Phase: N/A
Study type: Interventional

Postoperative pain stimulates the autonomic nervous system, induces the production of pro-inflammatory substances, reduces patient mobility and impairs vital functions. The ECG spectral analysis (ECGs) is a non-invasive marker of the autonomic nervous system state. To our knowledge, the correlation between the sympathovagal activity quantified by a non invasive method and the postoperative pain, has not been studied before.