Chirurgical Intervention

3

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

Condition / disease
Location
Status: Recruiting

Preoperative Use of Romiplostim in Thrombocytopenic Patients Undergoing Cardiac Surgery.

Romiplostim has demonstrated its efficacy and good tolerance in multiple indications. If the efficacy of Romiplostim is confirmed in this population, thrombocytopenic patients will be able to undergo cardiac surgery, which is generally life-saving, without prior thrombocytopenia. Patients included in the study will be hospitalized within 15 days of the first administration of the study treatment and will be closely monitored clinically and biologically for at least 10 days after surgery. The occurrence of an adverse event can therefore be quickly detected and managed. Collectively, "Patient Blood Management" strategies are mainly focused on the management of preoperative anemia. If positive, this study will enrich the therapeutic arsenal available for optimizing patients in preparation for major surgery. As no major collective complications are expected, the collective benefit/risk ratio also appears favorable.

Participants needed: 136
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Nantes University HospitalUpdated: Apr 6, 2026Locations: 8
Eligibility criteria

Adult patients with no upper age limit, [+5]

Inability to administer the first injection of Romiplostim or Placebo within 10... [+28]

Status: Recruiting

Evaluation of the Effect of Reiki on Pain After Spinal Fusion

This study involves patients undergoing lumbar spine surgery (lumbar arthrodesis). It compares the effects of Reiki, an energy-based therapy, with conventional approaches to relieve postoperative pain. The goal is to determine whether this non-drug method can help reduce pain, limit the use of painkillers, and enhance patient comfort during recovery.

Participants needed: 60
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Clinique BizetUpdated: Feb 4, 2026Locations: 1
Eligibility criteria

- Subject aged 18 years or older; [+3]

Neuropathic patient [+5]

Status: Recruiting

Effects of Osteopathic Management on Disability and Quality of Life After Lumbar Arthrodesis

The aim of our study is to assess the effect of a combined physiotherapy and osteopathy treatment versus a placebo on the management of disability and quality of life after lumbar arthrodesis. This study will provide a better assessment of the use of osteopathy as a non pharmacological approach to post-operative management. For this purpose, We will analyze the effects of these two approaches, targeted and non-targeted osteopathy (TO vs. NTO), on patients' disability and quality of life after surgery.

Participants needed: 40
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Clinique BizetUpdated: Jan 6, 2026Locations: 1
Eligibility criteria

having experienced a lumbar arthrodesis (of one to three levels) four weeks befo... [+2]

neuropathic pain according to a DN4 score greater than or equal to 4/10, [+5]