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Surgical Procedure, Unspecified clinical trials

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NCT ID: NCT04202874 Active, not recruiting - Clinical trials for Surgical Procedure, Unspecified

A Trial Comparing Surgeon-administered TAP Block With Placebo After Midline Laparotomy in Gynecologic Oncology

Start date: October 1, 2020
Phase: Phase 3
Study type: Interventional

Multimodal opioid-sparing analgesia is recommended in order to prevent post-operative complications and shorten length of stay. Administration by the surgeon of local anesthetics in the abdominal wall after surgery for a suspected gynaecological malignancy will be studied. Eighty women above the age of 18 and undergoing a midline laparotomy for a suspected gynecologic malignancy will be recruited. Half of these women will received a Transversus Abdominis Plane (TAP) block using local anesthetics, and half will receive a placebo (saline water). The primary outcome studied will be the total dose of opioid in morphine equivalents received in the postoperative period. The primary hypothesis is that surgeon-performed TAP blocks reduce the need for opioids after surgery. Secondary outcomes including postoperative pain scores, postoperative nausea and vomiting rates, time to flatus, incidence of clinical ileus and time to discharge from hospital will also be recorded.

NCT ID: NCT04134975 Recruiting - Clinical trials for Surgical Procedure, Unspecified

Evaluation of the Contribution of Intraoperative Scans Coupled With the Navigation for the Precision of the Positioning of the Pedicle Screws During a Lumbar Spine Surgery: a Prospective Randomised Study

SCANRACH
Start date: October 16, 2018
Phase: N/A
Study type: Interventional

Investigators team propose to evaluate the impact of the use of intraoperative scanning coupled with Stryker navigation, compared to the conventional fluoroscopy technique, on the accuracy of pedicle screws, in instrumented spinal surgery, by a randomised prospective study, in terms of pedicular screw accuracy. We will also evaluate the radiation exposure of the neurosurgical team and the patient in these two techniques.

NCT ID: NCT04061629 Completed - Clinical trials for Surgical Procedure, Unspecified

Minimal Occlusive Pressure With Cuffed ETTs: The Effect of 3 Different Sizes of cETT on Intracuff Pressure in Children

Start date: September 18, 2017
Phase:
Study type: Observational

Based on standard and historical practice, the predictive size of the endotracheal tube (ETT) to be used in children has been based on various formulas. However, no study has clearly compared these formulas to determine the optimal size of cuffed ETTs. Furthermore, they were developed when using a polyvinylchloride cuff and not the thinner polyurethane cuff which is in common clinical use today. Hence, the purpose of this current study is to evaluate which of the currently available formulas most closely predicts the appropriate size of cuffed ETT to be used based not only on the fit within the trachea, but more importantly the intracuff pressure after the cuff is inflated to seal the airway.

NCT ID: NCT04043637 Completed - Clinical trials for Urinary Incontinence

Early Urinary Continence After Radical Prostatectomy: Surgical Procedure and Anatomic Landmarks

Start date: April 23, 2012
Phase:
Study type: Observational

This study describes how to perform a correct prostatic apex and membranous urethra in order to preserve all anatomical elements that are necessary to achieve a very fast urinary continence after open/laparoscopic/robotic radical prostatectomy, avoiding positive surgical margins at this level.

NCT ID: NCT04033705 Completed - Diabetes Mellitus Clinical Trials

DRIVE - Perioperative Period

DRIVE-Periop
Start date: June 11, 2019
Phase:
Study type: Observational

This study will investigate if the HbA1c result before surgery which assesses glucose control over the longer term, can accurately predict what happens to the glucose levels and glucose profile following surgery. This will be recorded using continuous glucose monitoring sensors which are worn by participants pre and post elective surgery.

NCT ID: NCT04028986 Active, not recruiting - Infertility, Female Clinical Trials

Esmya Versus Surgery Before IVF/ICSI

Start date: January 1, 2016
Phase:
Study type: Observational

Studying the possible outcome differences between surgery or medical treatment with ulipristalacetate (UPA) solely before 'in-vitro fertilisation/intracytoplasmic sperm injection' (IVF/ICSI) treatment in infertile couples.

NCT ID: NCT03970785 Completed - Clinical trials for Surgical Procedure, Unspecified

Intraoperative Fluorescence of Ganglogliomas and Neuroepithelial Dysembryoplastic Tumors

FLUOGOD
Start date: July 15, 2018
Phase:
Study type: Observational

One of the key issues of tumour brain surgeries is to clearly define the borders of the tumor. The investigators proposed to evaluate the feasibility of intraoperative fluorescein guidance. Patients will be identified from the list of patients operated on under fluorescence to collect clinical datas. Surgical videos will be analyzed to assess the presence of intraoperative fluorescence and its subjectively judged intensity. MRI data will be extracted from the radiological reports to assess quality extraction. No additional data will be produced

NCT ID: NCT03967769 Recruiting - Clinical trials for Surgical Procedure, Unspecified

Apneic Oxygénation by Nasal Canula During Infants Airway Management Study

Oxyeno
Start date: August 5, 2019
Phase: N/A
Study type: Interventional

This is a randomized clinical trial investigating the utility of apneic oxygenation via high flow nasal cannulae during airway management for infants general anaesthesia. Three groups will be compared, a control group at 0 L/min, a 0,2L/Kg/min and a 1L/Kg/min group. The primary outcome will be the time (in seconds) between onset of apnea and one of theses end-points : desaturation (SPO2 <95%) or Airway management completed.

NCT ID: NCT03957889 Completed - Clinical trials for Surgical Procedure, Unspecified

Students and Trainers' Evaluations Correlation

Start date: July 2016
Phase:
Study type: Observational

The delegation of procedures within the medical competence to the nurses can increase the effectiveness of the healthcare provided. The objectives of the study are (1) to assess the quality of training courses for delegated surgical procedures through implementation for graduate scrub nursing ("students") (2) and to evaluate the correlation between the evaluation of this training carried out by students and the self-assessment conducted by the faculty ("trainers").

NCT ID: NCT03857620 Active, not recruiting - Carcinoma Clinical Trials

Use of a Pre-Surgical Toolkit in Improving Surgical Care and Outcomes in Older Participants With Cancer

Start date: July 24, 2019
Phase: N/A
Study type: Interventional

This trial studies how well the use of a pre-surgical toolkit (OPTI-Surg) works in improving surgical care and outcomes in older participants with cancer. In many elderly patients, surgery can greatly affect physical condition and the ability to return to pre-surgery levels of physical functioning. Providing pre-surgical recommendations may help improve participants' recovery rate and functioning after surgery.