Clinical trials

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Condition / disease
Location
Status: Not yet recruiting

Parents' Knowledge and Attitudes Towards Vaccinating Their Children

Purpose: To identify and evaluate the factors that influence parents' attitudes towards vaccination. Objectives: 1. To assess parents' level of knowledge about vaccines 2. To assess parents' attitudes and behavior regarding vaccine administration. 3. To observe whether there is a link between various socio-demographic factors and their knowledge about vaccines. 4. To assess the relationship and communication between doctors and parents. 5. To evaluate the influence of the COVID-19 pandemic on parents' trust in vaccines. Method Distribution of questionnaires to parents of patients under 18 years of age admitted in the Emergency Children's Hospital, Cluj-Napoca, Paediatrics Clinic III. Collection of clinical data by applying questionnaires completed voluntarily by parents

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Iuliu Hatieganu University of Medicine and PharmacyUpdated: Jun 29, 2026
Eligibility criteria

Not listed

Status: Recruiting

The Impact of Anaesthesia on Inflammation and NETosis in Hepatocellular Carcinoma Resection

According to recent literature, liver disease causes approximately 2 million deaths annually; 1 million are attributed to the complications of cirrhosis, while the remaining deaths are caused by hepatocellular carcinoma (HCC). The latter currently ranks 16th among the leading causes of death worldwide. Current research focuses on investigating novel therapeutic modalities, optimizing surgical and anesthetic practices, and identifying biological biomarkers to predict disease progression and severity. In this study, we address radiofrequency ablation (RFA) with the goal of improving periprocedural prognosis, recurrence rates, and overall survival. Specifically, we will quantify the expression of NETosis, a relatively novel biomarker with potential therapeutic and prognostic value in HCC progression. NETosis is a regulated form of cell death through which granulocytes release decondensed chromatin and various proteases into the extracellular space, forming a web-like meshwork known as neutrophil extracellular traps (NETs). These structures are actively involved in hepatic tumorigenesis by promoting tumor growth and metastasis. Recent clinical data reveal that NETs play a key role in: Local tumor progression The incidence of hepatic metastasis Direct modulation of the immune response Hepatic ischemia-reperfusion injury Several recent studies demonstrate that the in vivo blockade of NETosis reduces tumor recurrence, mitigates the pro-inflammatory state, and serves as a valuable prognostic indicator in advanced liver disease \[2,3,4\]. To suppress NETosis expression and ultimately lower recurrence rates, our protocol evaluates the intraprocedural administration of 1% lidocaine followed by a continuous postoperative intravenous lidocaine infusion.

Participants needed: 100
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Iuliu Hatieganu University of Medicine and PharmacyUpdated: Jun 18, 2026Locations: 1
Eligibility criteria

patients with a hepatocellular carcinoma suitable for RFA [+2]

candidates for surgery [+9]

Status: Not yet recruiting

Using Routine Inflammatory and Metabolic Blood Tests (Bedside Included) to Predict Brain Injury in Children After Minor Head Trauma

Traumatic brain injury (TBI) poses significant strains on the paediatric population, for which the possible side effects of diagnostic imagistics could induce life-altering conditions. Routine inflammatory and metabolic biomarkers (complete blood count, C reactive protein, glucose) are frequently sampled in the paediatric patients admited within emergency departments, including the low-resource settings. This study aims to retrospectively document whether such routine blood biomarkers could predict a positive head CT scan and subsequently contribute to a prediction score, ment to enable more accurate decision on which minor TBI paediatric patients should be submitted to diagnotic imagistics.

Participants needed: 800
Trial details
Age: Up to 18Biological sex: AllType: ObservationalSponsor: Iuliu Hatieganu University of Medicine and PharmacyUpdated: Mar 31, 2026Locations: 7
Eligibility criteria

Mild TBI will be defined as GCS 14-15 or A (AVPU) upon admission [+2]

Patients with moderate (GCS 13-9 or V) or severe (GCS 8-3 or P,U) head trauma [+1]

Status: Recruiting

Continous Infusion of Nefopam for Patients Undergoing Pancreatoduodenectomy

The goal of this clinical trial is to determine whether continuous nefopam administration, as part of a multimodal analgesia strategy, reduces opioid consumption and improves patient satisfaction after pancreatoduodenectomy. The main questions are: Does nefopam administration reduce opioid consumption after pancreatoduodenectomy? Does nefopam administration reduce postoperative pain levels after pancreatoduodenectomy? Researchers will compare two other analgesic strategies, namely continuous lidocaine infusion and epidural analgesia, to assess whether they lead to better outcomes. Participants will complete the QoR-15 questionnaire and report their pain levels at predefined time points before and after surgery.

Participants needed: 93
Trial details
Phase: Phase 4Age: 18-80Biological sex: AllType: InterventionalSponsor: Iuliu Hatieganu University of Medicine and PharmacyUpdated: Mar 24, 2026Locations: 1
Eligibility criteria

Patients scheduled for elective pancreatoduodenectomy surgery [+1]

Refusal to participate [+7]

Status: Not yet recruiting

Synbiotic Supplement With Botanical Extracts for Gut Microbiota Balance in Irritable Bowel Syndrome

The goal of this clinical trial is to evaluate whether a synbiotic dietary supplement containing botanical extracts and multiple probiotic strains can improve gastrointestinal symptoms and modulate gut microbiota composition in adults diagnosed with Irritable Bowel Syndrome (IBS). The main questions it aims to answer are: Does supplementation with the synbiotic product improve functional gastrointestinal symptoms associated with IBS (e.g., bloating, abdominal discomfort, and bowel habit disturbances)? Does the intervention lead to measurable changes in gut microbiota composition and selected biological markers compared with baseline measurements? Participants will: undergo baseline evaluation including symptom assessment, blood tests, and stool sample collection for gut microbiota analysis; complete an 8-week observation period without intervention to establish baseline variability; take the synbiotic supplement once daily for 8 weeks; repeat clinical assessments, blood tests, and gut microbiota analysis during follow-up visits.

Participants needed: 8
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: Iuliu Hatieganu University of Medicine and PharmacyUpdated: Mar 16, 2026Locations: 1
Eligibility criteria

Adults aged ≥18 years [+5]

Known or suspected organic gastrointestinal disease explaining the symptoms (e.g... [+8]

Status: Recruiting

Attitudes Towards Deprescribing Medications in Cancer Patients and Impact of Educational Intervention by a Clinical Pharmacist

Participation in this study consists in responding to some questions from two questionnaires in Romanian about how participants feel about deprescribing, participants' treatment and how participants understand medical information. After that, participants will receive a brochure and watch a video with some basic information about medications and participants' involvement in treatment decisions and in the next visit for cancer treatment participants will be asked to answer questions from one of the initial questionnaire.

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Iuliu Hatieganu University of Medicine and PharmacyUpdated: Feb 13, 2026Locations: 1
Eligibility criteria

cancer patients in palliative treatment [+1]

cancer patients in curative treatment [+2]

Status: Recruiting

Electrocoagulation vs. Cold Knife Cutting in Joint Arthroplasty (Electrocoagulation vs Scalpel)

Comparison of clinical outcomes of electrocoagulation and non-electrocoagulation techniques in total hip and knee arthroplasty surgery

Participants needed: 700
Trial details
Age: 18-90Biological sex: AllType: ObservationalSponsor: Iuliu Hatieganu University of Medicine and PharmacyUpdated: May 1, 2025Locations: 1
Eligibility criteria

Patients who have given informed consent to the procedure [+2]

Contraindications for major surgery or anaesthesia [+6]