Laparoscopic Abdominal Surgery

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

Condition / disease
Location
Status: Not yet recruiting

Comparison of Short- and Long-term Outcomes Between Robotic and Laparoscopic Hemicolectomy of Right Colon Cancer : A Multicenter Propensity Score Matching Analysis

This is a retrospective, multicenter cohort study to compare short- and long-term outcomes between robotic and laparoscopic hemicolectomy of right colon cancer.

Participants needed: 4,000
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: The First Affiliated Hospital of Nanchang UniversityUpdated: Jun 19, 2025
Eligibility criteria

1.Underwent radical right hemicolectomy by Da Vinci robotic or laparoscopic surg...

1.Received neoadjuvant therapy prior to surgery 2.History of other malignancies...

Status: Not yet recruiting

Study on the Effects of Multimodal Analgesia Regimens on Postoperative Analgesia and Gastrointestinal Function Recovery After Laparoscopic Abdominal Surgery

This clinical trial aims to investigate the impact of multimodal analgesia regimens on postoperative pain management and gastrointestinal function recovery following laparoscopic abdominal surgery. The primary objectives are to determine: Which analgesic regimen is most effective in reducing postoperative pain? Which analgesic regimen is most effective in accelerating gastrointestinal function recovery? This study will compare epidural analgesia (EA), paravertebral block (PB), transversus abdominis plane block (TAP), and patient-controlled intravenous analgesia (PCIA) to identify the optimal method for pain control and the most beneficial for gastrointestinal recovery. Participants will receive one of the following treatments postoperatively: epidural analgesia, paravertebral block, TAP block, or patient-controlled intravenous analgesia. Rest pain (measured using the Numerical Rating Scale, NRS), dynamic pain (NRS), morphine equivalent consumption (mg), quality of sleep on the first night (Likert scale, 1-5), time to return of bowel function (h), time to recommence oral intake (h), time to first mobilization (h), quality of recovery (QoR, 0-15) on postoperative day 1, and length of hospital stay (days) will be recorded at 4, 8, 12, and 24 hours post-procedure.

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Xiaguang DuanUpdated: Jan 14, 2025
Eligibility criteria

>18 years old [+3]

History of previous abdominal surgery [+7]

Status: Not yet recruiting

The Impact of a Dexmedetomidine Perfusion on Intraoperative Remifentanil Consumption

Opioids analgesic are the gold standard for intraoperative pain management. Their short- and long-term adverse effect motivate anesthesiologists to explore opioid sparing strategies. Dexmedetomidine is a highly selective α2 adrenergic receptor agonist that could help minimize opioid consumption both intraoperative and postoperative due to its sedative, analgesic and sympatholytic properties. This new randomized controlled trial (RCT) will answer the question whether an intraoperative dexmedetomidine infusion compared to placebo has a clinically significant impact on intraoperative remifentanil consumption during a laparoscopic abdominal elective surgery.

Participants needed: 72
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Ciusss de L'Est de l'Île de MontréalUpdated: Nov 12, 2024Locations: 1
Eligibility criteria

ASA 1-3 [+1]

Patient refusal [+4]

Status: Not yet recruiting

Outcome-related Performance Evaluation Through Revision and Analysis of inTraoperative Events

The goal of this prospective, multicentric, observational, cohort study is to evaluate intraoperative adverse events (iAEs) through video-based assessment (VBA) across minimal invasive procedures performed in general surgery departments. The main questions it aims to answer are: * The prevalence, type, and severity of iAEs * Correlation between iAE and clinical outcomes * Correlation between iAE and surgical performance * Qualitative analysis of root cause analysis and mitigation strategies

Participants needed: 700
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCSUpdated: Oct 24, 2024Locations: 5
Eligibility criteria

Patients scheduled for elective minimally-invasive surgery in participating cent... [+2]

Surgery performed with palliative intent or under unplanned/emergency setting [+2]