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Complication of Treatment clinical trials

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NCT ID: NCT06451510 Recruiting - Quality of Life Clinical Trials

Knee Osteoarthritis in the Region of Norrbotten

KORN
Start date: September 1, 2020
Phase:
Study type: Observational [Patient Registry]

The goal of this observational study is to assess the prevalence of radiographic knee osteoarthritis and to report medium and long term functional outcomes secondary to tibia plateau fractures. The second aim was to investigate whether there were any risk factors associated with these outcomes.

NCT ID: NCT06301048 Completed - Clinical trials for Complication of Treatment

Effectiveness of Endoscopic Papillectomy With Stent for Treating Duodenal Papillary Adenoma

Start date: November 7, 2023
Phase:
Study type: Observational

This is a retrospective study, including 79 patients with duodenal papillary adenoma, who treated with Endoscopic Papillectomy (EP) at Beijing friendship hospital. The cohort included patients who underwent EP with or without Pancreatic Duct (PD) and Common Bile Duct (CBD) stent placement. The investigators assessed the outcomes of EP and the impact of stent placement on complications and recurrence rates.

NCT ID: NCT05903326 Completed - Effect of Drug Clinical Trials

Dexmedetomidine as a Sole Premedication for BMT Placement

BMT
Start date: February 11, 2022
Phase:
Study type: Observational

There is very little evidence or research documenting any single method of sedation/analgesia for myringotomy tube (BMT) placement as being more effective than others. This was a retrospective chart review conducted to determine if there were significant differences in efficacy of administered pre-operative Midazolam and Intraoperative IM Ketorolac (traditional) vs. pre-operative Dexmedetomidine alone for pain and emergence delirium management of children undergoing placement of BMTs. The current protocol was changed under the direction of anesthesia and team members who wanted to see what the outcomes of the new management plan were. The plan was a prospective chart review and for this project, 276 patient charts were reviewed, 154 patients received traditional anesthesia treatment and 122 received Precedex. Data analysis indicated that the patients who had received Dexmedetomidine had significantly higher FLACC scores (meaning better pain control) than those who received the traditional therapy. There was no difference in emergence delirium between the two groups.

NCT ID: NCT05892367 Completed - Clinical trials for Complication of Treatment

Transbrachial Access for Interventions in Patients With Peripheral Arterial Occlusive Disease

TBA
Start date: July 10, 2018
Phase: N/A
Study type: Interventional

The aim of the present study is an evaluation, whether an immobilization of the upper extremity by means of a positioning splint can help to reduce the incidence of local complications after transbrachial puncture for peripheral arterial interventions, or not.

NCT ID: NCT05886127 Recruiting - Biliary Obstruction Clinical Trials

Treatment of Postsphincterotomy Bleeding With a Novel Self-assembling Peptide Hemostatic Gel.

ERCPURA
Start date: August 1, 2022
Phase:
Study type: Observational

The aim of this observational study is to evaluate safety and efficacy of a novel self-assembling peptide hemostatic gel in reduction of bleeding after endoscopic sphincterotomy during ERCP (endoscopic retrograde cholangiopancreatography )

NCT ID: NCT05725967 Enrolling by invitation - Obesity Clinical Trials

Endoscopic Metabolic and Bariatric Therapies

EMBTs
Start date: July 8, 2022
Phase:
Study type: Observational [Patient Registry]

This is a prospective collection of data from adult patients who have had an endoscopic metabolic and bariatric endoscopy procedure (EMBT) for primary or revision surgical procedures for obesity.

NCT ID: NCT05708651 Not yet recruiting - Hypoxia Clinical Trials

Evaluation of Medical Device for Airway Patency During Sedation (SW01-2022)

Start date: February 2023
Phase: N/A
Study type: Interventional

The goal of this four-part preclinical [I-II] and clinical [III-IV] trial is to compare, with randomised crossover study design [I-IV], a new medical airway device with standard procedure (biteblock or no device) for upper airway patency during sedation with intravenous propofol [I-IV]. - Page 1 of 9 [DRAFT] - The two main questions it aims to answer are if this new airway device is superior to standard procedure with respect to - maintenance of spontaneous ventilation [I] and upper airway volumes [II] at moderate and deep steady-state levels of sedation in healthy volunteer study participants, and - fewer and less lasting bedside signs of respiratory depression [III-IV], and less adjuvant use of manual airway support [III-IV] during procedural sedation (PS) according to standard of care(SOC) in study patients scheduled for colonoscopy or ureteral catheterisation under PS. Owing to the crossover study design used throughout the trial, there are no comparison groups of study participants [I-II] or study patients [III-IV].

NCT ID: NCT05429060 Recruiting - Quality of Life Clinical Trials

A Prospective Evaluation of Hemorrhoidal Surgery Outcome in Istanbul

Start date: June 1, 2022
Phase:
Study type: Observational [Patient Registry]

This study aims to evaluate the effect of surgical treatments on the quality of life in hemorrhoidal disease. All available treatment methods will be included in this 1-year cohort which is going to collect data from a big metropol.

NCT ID: NCT05238506 Completed - Acute Appendicitis Clinical Trials

Lidocaine VS Hemodynamic, Metabolic and Hormonal Response

Start date: March 12, 2022
Phase: Phase 4
Study type: Interventional

Intravenous lidocaine - a potent local anesthetic with analgesic and anti- inflammatory properties has been shown to be an effective adjunct that reduces intra and postoperative opioid consumption and facilitates pain management in adults. In children population promising but limited evidence is available. The study has been planned to evaluate the efficacy of continuous intravenous infusion of lidocaine in alleviation of hemodynamic reaction to tracheal intubation, as well as metabolic and hormonal response to laparoscopic procedure in children.

NCT ID: NCT05195697 Recruiting - Clinical trials for Complication of Surgical Procedure

ACUTE-Acute Surgical Care- Risk Factors and Outcomes for Patients in Need of Acute Surgical Care

ACUTE
Start date: January 1, 2020
Phase:
Study type: Observational

Observational retrospective study of patients in need of acute surgical care admitted to Skåne University Hospital between 2009 and 2019.