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NCT ID: NCT05482061 Completed - Chronic Pain Clinical Trials

Predictors of Treatment Failure Pain Among Patients Gunshot Wounds

PTFPAPGW
Start date: February 24, 2022
Phase:
Study type: Observational [Patient Registry]

In patients with gunshot wounds during hostilities in Ukraine, 76.9% have negative results of pain treatment, which leads to its chronicity. Identifying predictors of negative pain outcomes in these patients may improve their treatment outcomes.

NCT ID: NCT05478668 Completed - Clinical trials for Chronic Pain, Widespread

Predictors of Pain Chronicity in Patients With Gunshot and Mine-explosive Wounds

PP?PGM-EW
Start date: February 24, 2022
Phase:
Study type: Observational [Patient Registry]

82.1% of patients with gunshot and mine-explosive wounds during hostilities in Ukraine have negative results of pain treatment, which leads to its chronicity. Identifying predictors of pain chronicity in these patients may improve their treatment outcomes.

NCT ID: NCT05478655 Completed - Chronic Pain Clinical Trials

Predictors of Treatment Failure Pain Among Patients With Mine-explosive Wounds

PTFPAPM-EW
Start date: February 24, 2022
Phase:
Study type: Observational [Patient Registry]

Mine-explosive wounds in the general structure of combat sanitary losses reach 25%. They are characterized by significant damage resulting in high intensity pain. In patients who received mine-explosive injuries in the conditions of hostilities, such pain has its own unique features. It is necessary to pay more attention to the problem of pain treatment in patients of this category, because about 87.2% of cases have negative results of treatment - it becomes chronic.

NCT ID: NCT05478642 Completed - Chronic Pain Clinical Trials

Influence of Psychological Status on the Results of Pain Treatment in Patients With Gunshot and Mine-explosive Wounds

IPSRPTPGaM-EW
Start date: February 24, 2022
Phase:
Study type: Observational [Patient Registry]

82.1% of patients with gunshot and mine-explosive wounds and wounds during hostilities in Ukraine have negative results of pain treatment, which leads to its chronicity. Examining the effect of psychological status on pain management outcomes in these patients may improve their treatment outcomes.

NCT ID: NCT05478629 Active, not recruiting - Clinical trials for Regional Anesthesia Morbidity

Safety of Regional Anesthesia in Ukraine: the Survey

Start date: October 25, 2021
Phase:
Study type: Observational

The common using of ultrasound navigation makes an opportunity to develop the regional anesthesia. Regional anesthesia reduces the length of stay in the hospital, reduces the intensity of perioperative pain and decrease opioid using. But systemic toxicity of local anesthetics (LAST) is a significant problem. Prevalence of LAST in Europe range from 0.04 to 1.8 cases per 100 thousand local anesthesia. No similar studies have been provided in Ukraine before, and there are no statistics on the LAST epidemiology. Goal of this survey - evaluation of the prevalence of LAST, the safety of regional anesthesia in Ukraine.

NCT ID: NCT05461833 Completed - Clinical trials for Irritable Bowel Syndrome

FMT for Post-infectious IBS

Start date: September 1, 2020
Phase: N/A
Study type: Interventional

Considering that PI-IBS is brought on by infection and gut microbiota may be associated with the onset of symptoms, the modification of altered gut microbiota with nonabsorbable antibiotics such as rifaximin-α or probiotics is often employed as first-stage treatment. Research in recent years has also shown the potential benefits of fecal microbiota transplantation (FMT) for IBS, which is the replacement of a sick recipient's gut microbiota with fecal material from a healthy donor. Even though the only officially approved indication for FMT at this time is recurrent Clostridium difficile infection, the effectiveness of FMT is nevertheless being studied for the treatment of other gastrointestinal and non-gastrointestinal pathologies including IBS. To date, several controlled and uncontrolled studies have been conducted to study the effectiveness of FMT for IBS, and most of them have demonstrated positive results. The investigators have not come across studies devoted to the study of the effectiveness of FMT in patients with PI-IBS in the available literature. So, the aim of the current study was to conduct single-centre, randomized clinical trial to assess the safety, clinical and microbiological efficacy of FMT in patients with PI-IBS.

NCT ID: NCT05451381 Completed - Clinical trials for Hemodynamic Instability

Vasopressor Requirements Depends on Sedation Strategy

Start date: August 1, 2017
Phase: N/A
Study type: Interventional

Most of the patients after cardiac surgery need sedation in the iCU. Sedation strategy could impact the incidence of vasopressor use.

NCT ID: NCT05451121 Completed - Respiratory Failure Clinical Trials

Effect of Sedation Strategy on Duration Mechanical Ventilation in Patient After Cardiac Surgery

Start date: July 1, 2017
Phase: N/A
Study type: Interventional

There is a direct relationship between the sedative agent and the duration of ventilation.

NCT ID: NCT05450497 Completed - Arrythmia Clinical Trials

Effect of Sedative Agent on Reducing the Frequency of Arrhythmia in the Patients After Cardiac Surgery

Start date: July 1, 2017
Phase: N/A
Study type: Interventional

Arrhythmias early in the recovery period after cardio thoracic surgery are common they develop in 11 to 40 percent of patients after coronary-artery bypass grafting. The right chose of sedative agent could decrease the level of arrhythmia incidence.

NCT ID: NCT05447780 Recruiting - Clinical trials for Lumbar Spinal Stenosis

Comparing General Anesthesia, General Anesthesia With ESP Block or TLIP Block in Patients Undergoing Lumbar Surgeries

Start date: April 18, 2022
Phase: N/A
Study type: Interventional

The regional methods of anesthesia for the neurosurgical operations of the spine and spinal cord reducing the needs for opioids intra operatively and reducing pain in the postoperative period, decrease the numbers of failed back syndrome.