NCT07431892Recruiting
Pain Evaluation Across Robotic and Laparoscopic Surgery for Colorectal Procedures
Source: ClinicalTrials.gov · Last updated 25 Feb 2026
Brief summary (registry, in English)
Minimally invasive surgery for colorectal conditions, such as laparoscopic or robotic surgery, has been shown to offer benefits over traditional open surgery. These benefits include less pain after surgery, shorter hospital stays, and fewer complications. This study aims to compare two types of minimally invasive surgery-laparoscopic and robotic surgery-to determine which approach results in less postoperative pain for patients undergoing colon or rectal surgery. The central hypothesis is that robotic surgery, due to its higher precision and reduced tissue trauma, will lead to lower pain levels after surgery. The study will enroll adult patients scheduled for elective colorectal surgery at the Hospital General Universitario Gregorio Marañón in Madrid. Participants will undergo either laparoscopic or robotic surgery based on clinical availability and surgical planning, as long as they meet all inclusion criteria under the hospital's enhanced recovery protocol (RICA program). Researchers will assess patients' pain levels at different time points after surgery (immediately after recovery, at 24, 48, and 72 hours, and at discharge) using validated pain scales. The use of pain medications, hospital stay duration, complication rates, and quality of life up to 12 months after surgery will also be measured. All patient data will be collected anonymously using a secure electronic system (REDCap). The study will last approximately 2 years and include about 80 patients (40 in each group). The results could help surgeons and hospitals choose the most effective surgical approach to reduce postoperative pain and improve patient recovery in colorectal surgery.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 80 (estimated)
- First submitted
- 1 Jul 2025
- Start date
- 1 Sept 2025
- Primary completion date
- 28 Feb 2026
- Lead sponsor
- Hospital Central de la Defensa Gómez Ulla
- Diseases
- Colorectal cancer
- NCT number
- NCT07431892
What you commit to
- Study type: Observational
- Planned participants: 80
- From 1 Sept 2025 to the primary completion date, 28 Feb 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients with a preoperative decision for open surgery
- Patients undergoing rectal surgery (partial or total mesorectal excision without protective stoma)
- Patients requiring multivisceral resection due to oncologic indications identified intraoperatively
Other illness
- Patients with inflammatory bowel disease requiring colorectal resection
- Current or past history of chronic opioid use or opioid abuse
- Current or past history of benzodiazepine use or abuse
- Chronic use of analgesics for other comorbid medical conditions
- Current or past history of recreational drug use or abuse
- Non-adherence to preoperative care protocols (e.g., premedication, fasting, carbohydrate loading, thromboembolism prophylaxis, antibiotic prophylaxis, anesthetic care guidelines)
Other
- Extraction incision different from Pfannenstiel approach
- Non-compliance with the RICA protocol, including:
- Lack of preoperative nutritional, nursing, anesthetic, or pharmacy evaluation
Who the study is looking for
- Adults aged 18 years or older
- Signed informed consent
- Meeting inclusion requirements of the hospital's Enhanced Recovery Protocol (RICA program), including:
- Adequate cognitive status
- ASA (American Society of Anesthesiologists) classification I, II, or III
- Elective colon surgery (right or left hemicolectomy) for malignant disease
- Planned laparoscopic or robotic surgical approach
- Preoperative evaluation completed as per RICA protocol (nutritional, nursing, anesthetic, and pharmacy assessments)
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University Hospital Gregorio Marañón Coordinator of this site? Confirm its status | Madrid | Spain | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.