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Completed

NCT Number: NCT07252817

Intensive Monitoring of Post-surgery Pain in Major Ambulatory Surgery

Moderate to severe acute postoperative pain (APP) during part of the postoperative period is a barrier that hinders the central objective of perioperative medicine, which is to achieve an optimal postoperative recovery process. Despite advances in perioperative medicine, a large proportion of post-operative patients continue to suffer from moderate to severe APS during many of the days of their convalescence. This poor control of APS, in addition to causing suffering and exposing the patient to an increased risk of complications, could impair the quality of post-surgical recovery , according to some authors. We therefore consider it to be of utmost interest in our field to corroborate whether the implementation of measures to better control DAP is related to a better quality of post-surgical recovery.

Currently, the growing trend to take into account the perspective of patients in their care has prompted the development of various patient-centred measurement tools that, among other aspects, assess the quality of post-surgical recovery. Several scales have been designed. The most widely used are the QoR-40, QoR-9 and QoR-15 scales. The latter, with a range of 0 to 150, was developed to simplify assessment, especially in telephone follow-ups, and has a reliability similar to its predecessor, the QoR-40.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Consorci Sanitari del Maresme

Mataró, Barcelona, 08304, Spain

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients ≥ 18 years old.
  • ASA I - III.
  • Scheduled for the surgeries: Laparoscopic or open inguinal hernia repairs, Laparoscopic cholecystectomies, Haemorrhoid surgeries, Knee arthroscopies, Shoulder arthroscopies.
  • Willingness to be contacted by telephone during the duration of the study.
  • Informed written consent to participate in this study.

Exclusion criteria

  • Lack of proficiency in Spanish.
  • Undergoing study or follow-up for moderate to severe cognitive impairment.
  • Pregnant or breastfeeding patients.
  • Patients on major opioid medication.
  • Patients with a history of dependence/abuse of alcohol or illicit drugs at present.
  • Patients under active follow-up by the chronic pain unit.

Treatment and study plan

Intensive monioring group

Other

Routine follow-up (telephone call on the morning after surgery) and Intensive follow-up of acute post-surgery pain (telephone call every day since pain resolution).

Standard monitoring group

Other

Routine follow-up (telephone call on the morning after surgery).

Primary outcomes

  1. Quality of Recovery

    Time frame: Baseline (pre-surgery) and 48 hours, 7 days and 14 days post-surgery

    Quality of Recovery (QoR15 test)

Secondary outcomes

  1. Pain Control by Visual Analogic Scale

    Time frame: Baseline (pre-surgery) and 48 hours, 7 days and 14 days post-surgery

    Visual Analogic Scale of pain. Range values: 0 (minium pain) thru 10 (maximum pain)

  2. Satisfaction of pain control

    Time frame: Baseline (pre-surgery) and 48 hours, 7 days and 14 days post-surgery

    A 4-level Likert scale will be used according to the patient's criteria: dissatisfied, slightly dissatisfied, fairly satisfied, completely satisfied.

  3. Adherence to prescribed analgesic treatment

    Time frame: Baseline (pre-surgery) and 48 hours, 7 days and 14 days post-surgery

    4-level Likert scale according to the patient's criteria: no adherence, low adherence, moderate adherence, and total adherence.

Sponsors and collaborators

Lead sponsor

Consorci Sanitari del Maresme

Other

Registry information

Official study title

Seguimiento Intensivo Del Dolor Postoperatorio en cirugía Mayor Ambulatoria: Estudio de Viabilidad y Resultados

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Nov 28, 2025
Registry last updated
Dec 5, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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