Splenectomy

8

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

Condition / disease
Location
Status: Recruiting

Stanford Program to Accelerate Robotic Children's Surgery

The goal of this clinical trial is to provide additional data to confirm safety and performance of the da Vinci Xi Surgical System in a human clinical setting. This pilot study is intended to provide an initial assessment to evaluate the feasibility, safety, and effectiveness for the utilization of the da Vinci Xi on pediatric and adolescent patients. This clinical trial will be conducted under the auspices of Stanford University's IRB approval.

Participants needed: 250
Trial details
Age: 6-21Biological sex: AllType: InterventionalSponsor: Stanford UniversityUpdated: Apr 30, 2026Locations: 1
Eligibility criteria

Subject is between 6 - 21 years of age (weighing at least 15 kilograms) [+4]

Subject with uncorrected coagulopathy [+5]

Status: Recruiting

Efficacy of Apixaban in the Treatment of Portal Vein Thrombosis Occurring More Than One Year After LS

The purpose of this study is to determine whether Apixaban is effective and safe in the treatment of portal vein thrombosis Occurring more than one year after laparoscopic splenectomy.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: Mar 31, 2026Locations: 1
Eligibility criteria

A clinical, radiological, or histologic diagnosis of cirrhosis of any etiology. [+9]

Hepatocellular carcinoma or any other malignancy. [+9]

Status: Recruiting

Efficacy of Apixaban in Treating Portal Vein Thrombosis Occurring More Than One Year After LSD

The purpose of this study is to determine whether Apixaban is effective and safe in the treatment of portal vein thrombosis Occurring more than one year after laparoscopic splenectomy and azygoportal disconnection.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: Mar 31, 2026Locations: 1
Eligibility criteria

A clinical, radiological, or histologic diagnosis of cirrhosis of any etiology. [+10]

Hepatocellular carcinoma or any other malignancy. [+8]

Status: Recruiting

Evaluation of the Effectiveness of an Educational Intervention in Splenectomized Patients

The absence or dysfunction of the spleen is associated with a substantially increased risk of invasive infections that may rapidly progress to fulminant sepsis, including overwhelming post-splenectomy infection (OPSI), a medical emergency with high mortality. Although the risk is greatest in the first two years after splenectomy, it persists lifelong. Preventing infections in patients with anatomical or functional asplenia requires an integrated strategy that includes patient education, early recognition of symptoms, behavioral measures, antibiotic prophylaxis when indicated, and vaccination. Post-splenectomy immunization has been shown to reduce OPSI incidence. Regional and international guidelines recommend vaccination against pneumococcus, Haemophilus influenzae type b, meningococcus (B and ACWY), herpes zoster, diphtheria-tetanus-pertussis, measles-mumps-rubella-varicella, and annual influenza. However, adherence to these recommendations is frequently suboptimal, often due to limited awareness among patients and healthcare professionals. This study involves the intra-hospital vaccination team providing structured vaccination consultations to splenectomized patients hospitalized at the Fondazione Policlinico Universitario "A. Gemelli" IRCCS. During ward consultations, patients receive an educational intervention on asplenia-related infectious risks and preventive measures, supported by standardized informational materials. Effectiveness is evaluated using a pre-post questionnaire assessing knowledge and awareness. Patients completing the vaccination pathway at the outpatient clinic also complete a questionnaire assessing their experience with vaccination management in an intra-hospital setting.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCSUpdated: Feb 2, 2026Locations: 2Duration: 24 Months
Eligibility criteria

Adult patients (≥18 years old) [+2]

Minor patients [+2]

Status: Recruiting

Research Trial Assessing the Immunogenicity and Safety of Three Meningococcal B Vaccine Strategies Among Patients With Asplenia.

The purpose of the study is to evaluate the immunological response and tolerance of 3 vaccine strategies against meningococcus B, a potentially fatal invasive infection.

Participants needed: 84
Trial details
Phase: Phase 3Age: 18-75Biological sex: AllType: InterventionalSponsor: Assistance Publique - Hôpitaux de ParisUpdated: Nov 20, 2025Locations: 1
Eligibility criteria

Male or female, >=18 to <=75 years old. [+6]

History of meningococcal vaccination B. [+12]

Status: Recruiting

Physiology and Pathologies Linked to Human Splenic Function : Direct and Ex-vivo Perfusion Explorations

Human splenic physiology remains poorly understood due to lack of functional exploration. However, through its ability to recognize alterations or modifications in circulating cells and to trigger an innate and adaptive response in response to these anomalies, the spleen plays a central role in several diseases affecting blood cells, directly or indirectly. The analysis of the splenic clearance of abnormal cells during ex-vivo perfusions made it possible to clarify the pathogenesis of malaria and the role of the spleen in the adaptive immune response. The study's investigative team wishes to extend these explorations to other human diseases in which the spleen is involved, and to evaluate the preventive or curative potential of substances that can modify the perception of blood cells by the spleen (e.g. monoclonal antibodies directed against circulating cells, among other options).

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Assistance Publique - Hôpitaux de ParisUpdated: Sep 15, 2025Locations: 5
Eligibility criteria

Adult patients [+1]

Status: Not yet recruiting

Study of the Prevalence of Acid Sphingomyelinase Deficiency/Niemann Pick AB and B Disease in Patients With Diffuse Interstitial Lung Disease

The goal of this clinical trial is to optimise and facilitate screening for Acid SphingoMyelinase Deficiency (ASMD) disease, by evaluating acid sphingomyelinase activity and, where appropriate, LysoSM levels in a cohort of 200 participants with diffuse interstitial lund disease (ILD) at risk of developing ASMD disease. ILD is common in the general population, so in order to limit the number of differential diagnoses, the population to be studied will be restricted to participants aged between 15 years and 3 months and 60 years, with ILD plus ground-glass opacities on chest CT scan certified by a pulmonologist/radiologist or internist, AND splenomegaly or splenectomy, and/or thrombocytopenia, and/or low HDL cholesterol, and/or parental consanguinity which increase the sensitivity of ASMD screening. In this clinical trail, two procedures are added, participants will be asked for : * a blood sample to measure the acid sphingomyelinase enzyme activity and LysoSM, if required. * a follow-up visit at 6 months

Participants needed: 200
Trial details
Age: 15-60Biological sex: AllType: InterventionalSponsor: Wladimir MAUHIN, DrUpdated: May 18, 2025Locations: 1
Eligibility criteria

Interstitial lung disease with ground-glass lesions on a chest CT scan certified... [+7]

Inability to understand the information provided. [+2]

Status: Recruiting

Evaluation of Immune Status Before and After Splenectomy in Immune Thrombocytopenia Patients

Evaluation of immune status before and after splenectomy in immune thrombocytopenia patients.

Participants needed: 50
Trial details
Age: 18-60Biological sex: AllType: ObservationalSponsor: Institute of Hematology & Blood Diseases Hospital, ChinaUpdated: Feb 24, 2025Locations: 1
Eligibility criteria

Aged 18 to 60 years old, male or female; [+3]

Secondary thrombocytopenic purpura; [+2]