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Research institution

Tampere University Hospital Clinical Trials

Studies where Tampere University Hospital is the lead sponsor: what is enrolling now, by phase, condition and country.

212 registered studies

In numbers

Open to volunteers
50
Active
58
With results posted
2
All registered
212

Open to volunteers: recruiting, not yet recruiting or enrolling by invitation. Active adds studies under way that have stopped recruiting.

Open to volunteers

All 50
  • Colorectal Cancer

    T1 Colorectal Cancer After Local Excision: Decision Between Surgery and Active Surveillance (T1LDA Trial)

    • Not yet recruiting
    • Age: 18 years and older
    • Surgery or procedure

    The goal of this two-arm clinical trial is to compare additional surgery with active surveillance in patients with high-risk pT1 colorectal cancer after local excision.

    Trial name
    T1LDA (NCT07900620)
    Testing
    Additional surgery
    Where
    14 sites in Finland
    Volunteers
    500 people
    Sponsor
    Tampere University Hospital
    Can I take part? T1LDA
  • Wrist Ganglion, Ganglion

    Ganglion Resection Effectiveness Trial

    • Recruiting
    • Age: 18 years and older
    • Surgery or procedure

    The goal of this clinical trial is to learn if surgery helps with wrist ganglions in adults. The main question it aims to answer is: Does surgery result in better patient-reported outcomes and satisfaction over a 6-months…

    Conditions
    Wrist Ganglion, Ganglion, Ganglion Cyst, Connective Tissue Disease
    Trial name
    GangLion (NCT07162415)
    Testing
    Open resection, Arthroscopic resection, Conservative treatment
    Where
    6 sites in Finland, Singapore
    Volunteers
    220 people
    Sponsor
    Tampere University Hospital
    Can I take part? GangLion
  • Obstetric Anal Sphincter Injury, Sexual Dysfunction and the Mode of Deliveries

    Long-term Pelvic Floor and Sexual Health After Obstetric Anal Sphincter Injury in Finland

    • Enrolling by invitation
    • Age: 18 years and older
    • Observational study

    The goal of this observational study is to understand long-term pelvic floor symptoms and sexual dysfunction after childbirth-related anal sphincter injury in women who gave birth at Tampere University Hospital between 2009 and…

    Conditions
    Obstetric Anal Sphincter Injury, Sexual Dysfunction and the Mode of Deliveries, Pelvic Floor Disorders
    Trial name
    NCT07646340
    Where
    Finland
    Volunteers
    600 people
    Sponsor
    Tampere University Hospital
    Can I take part? NCT07646340
  • Healthy, Newborn Infant

    Smart Sock Heart Rate Monitoring in Hospitalized Newborns

    • Enrolling by invitation
    • Age: 0 to 28 days
    • Observational study

    The goal of this observational study is to evaluate a commercially available smart sock for heart rate monitoring in hospitalized newborn infants without known heart disease.

    Trial name
    NCT07838402
    Where
    Finland
    Volunteers
    40 people, healthy volunteers welcome
    Sponsor
    Tampere University Hospital
    Can I take part? NCT07838402
  • Iron Deficiency Anaemia in Childbirth, Iron Deficiency

    Maternal Iron Deficiency and Childhood Health

    • Recruiting
    • Age: All ages
    • Observational study

    The aim of this prospective observational cohort study is to study maternal iron deficiency and iron deficiency anemia and the use of iron supplements in pregnancy and their impact on the health of the offspring and pregnancy…

    Conditions
    Iron Deficiency Anaemia in Childbirth, Iron Deficiency, Iron Deficiency in Pregnancy, Iron Deficiency Anemia in Pregnancy
    Trial name
    MATILDA (NCT06879080)
    Where
    Finland
    Volunteers
    6,000 people, healthy volunteers welcome
    Sponsor
    Tampere University Hospital
    Can I take part? MATILDA
  • Carpal Tunnel Syndrome

    Effect of Night-time and Full-time Splinting for Carpal Tunnel Syndrome

    • Recruiting
    • Age: 18 years and older
    • Medical device

    Carpal tunnel syndrome is a common compression neuropathy of upper extremities. Its usual symptoms are pain, numbness and tingling of fingers, which tend to be worse at night.

    Trial name
    FINCROSS (NCT05637294)
    Testing
    splinting
    Where
    6 sites in Finland
    Volunteers
    110 people
    Sponsor
    Tampere University Hospital
    Can I take part? FINCROSS
  • Rectal Cancer, Rectal Adenocarcinoma

    Nordic ORgan Preservation Pilot Approach Nonrandomised Single-Arm Trial for Non-Operative Management of Rectal Cancer

    • Recruiting
    • Age: 18 years and older
    • Surgery or procedure

    The goal of this one-arm clinical trial is to implement and study the oncological outcomes of nonoperative management of rectal cancer having complete clinical response to neoadjuvant therapy.

    Trial name
    NORPPA-1 (NCT06328361)
    Testing
    Nonoperative surveillance
    Where
    13 sites in Estonia, Finland
    Volunteers
    200 people
    Sponsor
    Tampere University Hospital
    Can I take part? NORPPA-1
  • Ulcerative Colitis (UC), Primary Sclerosing Cholangitis (PSC)

    Vancomycin Efficacy in Response to Dysbiosis in Atypical Colitis

    • Not yet recruiting
    • Age: 6 to 15 years
    • Phase 2
    • Pill or oral medicine

    The goal of this clinical trial is to learn how oral vancomycin therapy may contribute in treating paediatric inflammatory bowel disease, particularly atypical ulcerative colitis and PSC-associated colitis.

    Conditions
    Ulcerative Colitis (UC), Primary Sclerosing Cholangitis (PSC), Pediatric Inflammatory Bowel Diseases
    Trial name
    VERDA (NCT07646223)
    Testing
    Oral Vancomycin
    Where
    Finland
    Volunteers
    140 people
    Sponsor
    Tampere University Hospital
    Can I take part? VERDA
  • IBD (Inflammatory Bowel Disease)

    E-nose in Evaluating Colitis Activity

    • Not yet recruiting
    • Age: 1 year to 16 years
    • Observational study

    The goal of this observational study is to learn whether a rapid stool-based imaging test can help monitor inflammatory bowel disease (IBD) in children.

    Trial name
    SPECTROS (NCT07781215)
    Testing
    Differential Mobile Spectrometry analysis of the stool
    Volunteers
    120 people, healthy volunteers welcome
    Sponsor
    Tampere University Hospital
    Can I take part? SPECTROS
  • Obsessive Compulsive Disorder (OCD)

    Bergen Four-Day Treatment (B4DT) for Obsessive-Compulsive Disorder

    • Recruiting
    • Age: 18 years and older

    The aim of this study is to expand access to Bergen Four-Day Treatment (B4DT) in Finland and to integrate it into psychiatric care pathways at Tampere University Hospital (TAYS).

    Trial name
    NCT07644130
    Testing
    Bergen Four-Day Treatment (B4DT)
    Where
    Finland
    Volunteers
    65 people
    Sponsor
    Tampere University Hospital

Completed, with results posted

All 2
  • Postoperative Pain

    Clinical Analysis of Pain After Hysterectomy

    • Completed
    • Age: 18 to 69 years
    • Observational study
    • Results posted

    Patients undergone either laparoscopic or vaginal hysterectomy will called for a clinical examination 1-3 years after surgery, if they suffer from pain 6 months after surgery. The aims of the study are: 1.

    Trial name
    NCT01706549
    Where
    Finland
    Volunteers
    16 people
    Sponsor
    Tampere University Hospital
    Can I take part? NCT01706549
  • One-year Outcome After Prehospital Intubation

    One-year Outcome After Prehospital Intubation

    • Completed
    • Age: All ages
    • Observational study
    • Surgery or procedure
    • Results posted

    The primary aim of this study was to describe the long-term outcome of critically ill or severely injured patients not in cardiac arrest treated by an EMS physician.

    Trial name
    NCT02307123
    Testing
    Intubation
    Volunteers
    483 people
    Sponsor
    Tampere University Hospital
    Can I take part? NCT02307123

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