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Pain clinical trials

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NCT ID: NCT05688410 Recruiting - Pain Clinical Trials

Enhancing Exercise and Psychotherapy to Treat Pain and Addiction in Adults With an Opioid Use Disorder (EXPO; R33 Phase)

EXPO-R33
Start date: February 10, 2023
Phase: N/A
Study type: Interventional

This work will involve conducting a randomized trial that will evaluate preliminary efficacy of "assisted" rate cycling, voluntary rate cycling and psychotherapy for pain individually and in combination as adjunctive treatments on cravings (primary outcome) in adults with an opioid use disorder. The investigators will also evaluate the effects of "assisted" rate cycling, voluntary rate cycling and I-STOP on secondary outcomes including depression, anxiety and sleep.

NCT ID: NCT05688384 Recruiting - Pain Clinical Trials

Patient-Controlled Sedation in Port Implantation (PACSPI-2)

PACSPI-2
Start date: January 19, 2023
Phase: Phase 4
Study type: Interventional

The goal of the study is to determine if patient-controlled sedation (PCS) with propofol and alfentanil reduces patient-reported pain perception during implantation of subcutaneous venous port (SVP). The main question it aims to answer: How much pain did you (patient) experience during SVP-implantation Several other questions will be answered regarding: patient´s perception of the procedure, complication rate, procedure data. The study contains two groups which will be compared. Control group: will do SVP implantation under local anaesthesia Study group: will do SVP implantation under local anaesthesia and patient-controlled sedation. The patients are asked to complete a questionnaire postoperatively which contains questions on pain perception and satisfaction.

NCT ID: NCT05686148 Recruiting - Pain Clinical Trials

The Effect of Vibration Application on Pain and Satisfaction Associated With Subcutaneous Anticoagulation Injection

Start date: September 20, 2022
Phase: N/A
Study type: Interventional

This study was needed to relieve the pain associated with subcutaneous injection, which is an application performed by nurses, to increase patient satisfaction, to increase patient compliance with treatment, and to strengthen positive patient-nurse communication. The purpose of this study is to assess the effect of vibration stimulation application on subcutan injection induced pain and patient satisfaction. The study will be carried out in the internal medicine service of a university hospital. Vibration will be applied during subcutaneous injection of anticoagulant to one group, but not to the other group. It was planned to include 85 patients in the study.

NCT ID: NCT05684939 Completed - Pain Clinical Trials

Relation Between Substance Use and Pain, in Patients Suffering or Surviving From Cancer and Followed in France

CAPS
Start date: January 27, 2023
Phase:
Study type: Observational

Pain is one of the most prevalent symptoms during and after cancer. Pain can be the consequence of several situations (disease progression, surgery, and anticancer drugs). However, pain can frequently be associated with a substance use disorder (alcohol, tobacco, drugs, and illicit products such as cannabis). The relationship between substance use and pain is known to be complex and interdependent, i.e. pain can reinforce substance use and substance use can promote pain. However, few data in the literature are available on the use of psychoactive substances in relation to pain in the context of cancer (cancer patients and cancer survivors). Moreover, the scientific literature agrees on the fact that these elements are little studied and underestimated in the clinic. The investigators hypothesize that, in cancer patients or cancer survivors, the prevalence of the use of psychoactive substances would be higher in the presence of pain, and would be associated with its intensity and its impact on the quality Health-Related Living (HRQoL). The main objective of this study will be to compare, in an adult population of patients suffering from cancer or having had cancer, the prevalence of the consumption of psychoactive substances in painful patients compared to non-painful patients.

NCT ID: NCT05684471 Completed - Pain Clinical Trials

SFIB vs Anterior QLB in Total Hip Arthroplasty

Start date: January 18, 2023
Phase: N/A
Study type: Interventional

Quadratus lumborum block (QLB) is a facial plane block defined to provide analgesia from T7-L3 dermatomes. There are articles reporting that it is an effective analgesic method in hip surgeries. Suprainguinal fascia iliaca block (SIFIB) also blocks components of the lumbar plexus and provides effective analgesia in hip surgeries. The investigators aim to compare the effectiveness of QLB and SIFIB in patients undergoing primary total hip arthroplasty (THA).

NCT ID: NCT05682235 Active, not recruiting - Endometriosis Clinical Trials

Therapeutic Exercise and Education in Pain Neurophysiology to Improve Pain Intensity in Women With Endometriosis. Clinical Trial.

Start date: December 12, 2022
Phase: N/A
Study type: Interventional

The objective of this study will be to evaluate treatment using ET exercise and pain education in women with endometriosis to improve pain intensity.

NCT ID: NCT05680259 Recruiting - Pain Clinical Trials

Assessment of the Effects of Maela Connected Follow-up on Well-being and Pain After Lumbar Spine Surgery

HOSPITEL
Start date: October 6, 2022
Phase: N/A
Study type: Interventional

Digital technologies could reduce the length of hospital stay and improve post-operative recuperation after discharge by offering a remote follow-up. No study has investigated the effects of connected follow-up on lumbar spine inpatients. The purpose of this project is to assess the effects of connected follow-up on pain and quality of life after lumbar spine surgery.

NCT ID: NCT05679947 Completed - Pain Clinical Trials

Mobilization Protocol for Knee Arthroplasty Patients

KA-Mobility
Start date: May 1, 2022
Phase: N/A
Study type: Interventional

This randomized controlled study evaluates the effect of mobilization protocol applied to knee arthroplasty patients on anxiety level, pain, mobility and functional status.

NCT ID: NCT05679726 Completed - Pain Clinical Trials

The Effect of Foot Reflexology in Intensive Care Nurses

Start date: November 1, 2022
Phase: N/A
Study type: Interventional

This study was planned as a randomized controlled experimental research design to examine the effect of foot reflexology applied to nurses working in the intensive care unit on stress, fatigue and low back pain.

NCT ID: NCT05678296 Completed - Pain Clinical Trials

Investigation of Effectiveness of Local Antibiotic With Platelet Rich Fibrin on Third Molar Surgery Outcomes In Vivo

Start date: April 20, 2020
Phase:
Study type: Observational

The aim of this study was investigate the effectiveness of Local Antibiotic Applications With Platelet Rich Fibrin on Third Molar Surgery Outcomes In Vivo and In Vitro. The study included a total of 60 patients with impacted mandibular third molar. Patients were evaluated in 3 randomly separated groups. For the first and second group, Platelets Rich Fibrin+ local antibiotics were applied into the tooth socket. For the first group, amoxicillin was applied and for the second group, clindamycin was applied. There was a control group which only Platelets Rich Fibrin was applied into the socket. The outcome variables were pain, swelling, the number of analgesics taken, and trismus. These variables were also assessed based on first, second, third, and seventh days following the operation.