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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: 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: 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.

NCT ID: NCT00273169 Completed - Postoperative Clinical Trials

Use of the PSA 4000 Monitor in the Post-Operative Period in Patients Undergoing Major Surgery

Start date: July 2005
Phase: N/A
Study type: Observational

Evaluate correlation between the values from the PSA monitor and clinical assessment of sedation with the RASS on postoperative patients.

NCT ID: NCT00235261 Completed - Pain Clinical Trials

Effect of Paracetamol, Pregabalin and Dexamethasone on Pain and Opioid Requirements in Patients After Hip Operations

Start date: October 2005
Phase: Phase 4
Study type: Interventional

Patients scheduled for primary total hip replacement needs postoperative pain treatment: i.e. morphine. Unfortunately morphine has side-effects: nausea, vomiting, sedation and dizziness, which is unpleasant for the patients and sometimes keeps them at bed longer time than needed. We investigate in new combinations of analgesics for postoperative pain, hoping to minimize the need for morphine and improve the patients pain score after operation.

NCT ID: NCT00150865 Completed - Pain Clinical Trials

Evaluation of Efficacy of Lumbar Plexus Bloc After Hip Surgery

Start date: September 2001
Phase: N/A
Study type: Interventional

Compare lumbar plexus block with ropivacaine 0.475%, 0.4 ml/kg to saline. Each group randomized, includes 30 patients. block performed preoperatively Surgery under general anesthesia. Postoperative evaluation of pain (VAS) as first endpoint, and also morphine consumption via PCA device. Follow-up : 24h. Expectation : sizeable reduction of pain with block, of duration.