Anesthesia Complication

9

Review clinical trials related to Anesthesia Complication. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Determinants of Technical Success and Safety in Therapeutic ERCP for Obstructive Jaundice

compare the impact of type of anesthesia on ERCP including technical success, rate of complications, peri procedural safety, patient and endoscopist satisfaction in adult patients with obstructive jaundice

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Sohag UniversityUpdated: May 4, 2026
Eligibility criteria

Adult patients above 18 years old. [+2]

Patients below 18 years old. [+5]

Status: Recruiting

Complications Related to the Anaesthesia During Airway Endoscopy in Children With Tracheostomy.

The goal of this observational study is to investigate the incidence of severe anaesthesiologic complications during anaesthesia in children with tracheostomy undergoing surveillance airway endoscopy. The main question it aims to answer is how common severe anaesteshiologic complications are in these patients and investigate if there is an association between severe anaesthesiologic complications and patient related factors. Primary outcome: The incidence of severe anaesthesiologic complications in children with tracheostomy undergoing surveillance airway endoscopy. Secondary outcome: The association between severe anaesthesiologic complications and patient related factors: age at tracheostomy, age at surveillance endoscopy, ventilator dependence, current and previously diagnosed tracheostomy related airway complications. All children under 18 yrs. of age with a tracheostomy accepted for general anaesthesia undergoing surveillance airway endoscopy at the Long term Intensive Care unit at Karolinska University Hospital Stockholm Sweden will be eligable for inclusion. The anaesthesia will be conducted according to current practise and complications will recorded by the anaesthesiologist in charge. Participants may only be included several times during the study period.

Participants needed: 80
Trial details
Age: Up to 18Biological sex: AllType: ObservationalSponsor: Karolinska InstitutetUpdated: Mar 20, 2026Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Propofol and Etomidate Admixtures Comparisons Trial (PEAC Trial)

The purpose of this study is to evaluate the hemodynamics and adverse event profile in comparison between two treatment arms, one using an admixture of propofol and etomidate at a ratio by volume of 25%/75% (P2E7), and one using an admixture of propofol and etomidate at a ratio by volume of 75%/25% (P7E2), for anesthesia during endoscopic procedures at the Clements University Hospital (CUH) endoscopy lab (Endo).

Participants needed: 200
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: University of Texas Southwestern Medical CenterUpdated: Jan 20, 2026Locations: 1
Eligibility criteria

Adult patients (age ≥18 years old) [+3]

Known allergies or adverse reactions to study drugs or study drug components or... [+5]

Status: Recruiting

Trajectories of Recovery After Intravenous Propofol Versus Inhaled VolatilE Anesthesia Trial

The investigators will conduct a 13,000-patient randomized multi-center trial to determine (i) which general anesthesia technique yields superior patient recovery experiences in any of three surgical categories ((a) major inpatient surgery, (b) minor inpatient surgery, (c) outpatient surgery) and (ii) whether TIVA confers no more than a small (0.2 %) increased risk of intraoperative awareness than INVA in patients undergoing both outpatient and inpatient surgeries

Participants needed: 13,000
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Washington University School of MedicineUpdated: Aug 5, 2025Locations: 20
Eligibility criteria

Aged 18 years or older [+1]

Inability to provide informed consent in English (at all study sites) or Spanish... [+8]

Status: Recruiting

Perioperative Management Evaluation in Patients With CIED

Background: Recommendations for peri-operative management in patients with implanted cardiac electronic devices (CIED) are often based on older data from case reports and small collectives. Objective: To evaluate the peri-operative management and outcome of patients with implanted CIED undergoing non-CIED related surgery or catheter-interventional procedures in clinical routine. Study design: bi-center, non-randomized, observational registry, retrospective data-collection, on-going prospective patient enrollment, descriptive statistics Primary endpoint: number and type of peri-operative adverse device related events (ADE) Secondary endpoints: pre-interventional data (patient characteristics, data from CIED interrogation); peri-interventional data (type of surgery/intervention, anesthesiology techniques, any AE), postinterventional data (data from post-interventional CIED interrogation, need for reprogramming / device revision). Inclusion criteria: implanted CIED, non-CIED related surgical or catheter-based intervention, peri-procedural CIED interrogation, age \>18 years Exclusion criteria: no implanted CIED, no data from any peri-procedural CIED interrogation available Patient enrollment: retrospectively beginning from 2008, further on-going prospective inclusion Sample size: For the observational study, there is no pre-specified sample size. Data from more than 500 patients undergoing \> 700 interventions are expected.

Participants needed: 500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Klinikum-FuerthUpdated: Oct 15, 2024Locations: 2Duration: 1 Month
Eligibility criteria

implanted CIED (e.g. pacemaker, ICD, CRT), [+3]

no implanted CIED, [+1]

Status: Recruiting

Preoperative Blood Volume Optimization Using Transthoracic Echocardiography

Immediately following the induction of general anesthesia, arterial hypotension may occur with an incidence of about 40% in patients classified as ASA 3 or 4. Perioperative arterial hypotension is associated with increased perioperative morbidity and mortality. The increased mortality associated with perioperative arterial hypotension has been reported up to 30 and 90 days after surgery. This association appears to be both dose-dependent and time-dependent (severity and duration of arterial hypotension). EchOptimal study aims to determine whether non invasive preoperative stroke volume optimization using transthoracic echocardiography (TTE) can reduce the incidence and severity arterial hypotension following induction of general anesthesia. This is prospective, randomized, controlled, double blinded study approved by ethics comittee. The primary objective of this study is to compare the incidence of arterial hypotension (mean arterial pressure \< 65 mmHg) within the first 15 minutes following the induction of general anesthesia, between 2 groups : * standard current care (stroke volume optimized after induction of general anesthesia using oesophageal doppler) and * preopertaive stroke volume optimization using transthoracic echocardiography measument of subaortic velocity time integral.

Participants needed: 220
Trial details
Age: 18-99Biological sex: AllType: InterventionalSponsor: University Hospital, CaenUpdated: Oct 15, 2024Locations: 1
Eligibility criteria

Patient aged 18 years or older, [+5]

Patients under guardianship, curatorship, judicial protection, or legal protecti... [+10]

Status: Recruiting

PCV-VG in Pediatric Laparoscopic Surgery

This Study will aim to compare the effects of Pressure Controlled Ventilation - Volume Guarantee (PCV-VG) mode with volume control ventilation (VCV) and pressure control ventilation (PCV) modes on respiratory mechanics (including the dynamic compliance, PIP, mean airway pressure, driving pressure..etc) and oxygenation in pediatric laparoscopic surgery.

Participants needed: 75
Trial details
Age: 1-8Biological sex: AllType: InterventionalSponsor: Assiut UniversityUpdated: Jul 30, 2024Locations: 1
Eligibility criteria

ASA physical status I-II. [+4]

ASA physical status more than II. [+6]

Status: Not yet recruiting

This Study Assess Some Physiological Parameters, Blood Picture, and Hemodynamic Parameters, Blood Pressure, Respiratory Assess by SPO2, During Different Periods in Laparoscopic Surgery

Laparoscopic surgery is widely used now. These benefits included many items, e.g. reducing post-operative pain, cosmetic the result was improved, and the patient also had more satisfaction for the patient and reduced hospital stay. This surgery involved insufflation of gas into the peritoneal cavity, producing pneumoperitoneum, and causing an increase in intra-abdominal pressure. The raised intraabdominal pressure of the pneumoperitoneum, the patient's position alteration, and the absorption of carbon dioxide into the abdomen have a direct effect on causing a change in physiology, especially in the cardiovascular and respiratory systems. These effects, as well as a direct effect of gas insufflation, may have significant effects on the patient especially if the patient has a comorbidity or is elderly.

Participants needed: 60
Trial details
Age: 20-60Biological sex: AllType: InterventionalSponsor: Mohammed AbdulhameedUpdated: Jun 25, 2024
Eligibility criteria

elective abdominal surgery [+3]

emergency condition [+1]

Status: Not yet recruiting

Registry of Anesthesia and Perioperative Medicine

To assess mortality and morbidity associated to anesthesia interventions

Participants needed: 10,000
Trial details
Biological sex: AllType: ObservationalSponsor: Clinica Alemana de SantiagoUpdated: May 22, 2023Locations: 1Duration: 1 Year
Eligibility criteria

All individuals [+1]

The subjects who had insufficient data in their files