NCT07169604

Completed

Analgesia Robotic Gynaecological Surgery

Fondazione Policlinico Universitario Agostino Gemelli IRCCS Source

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Other study identifiers

Sponsor study identifier

3307

Study Type

observational

Actual enrollment (reported)

100

Locations

1 country

Sites

1

Timeline

Study Start

January 1, 2021

Actual (reported)

Primary Completion

December 1, 2024

Actual (reported)

Study Completion

December 1, 2024

Actual (reported)

Brief Summary

we will retrospectively investigate the effect of intratecal morphine administration on postoperative pain relief for patients scheduled for robotic hysterectomy

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 100 participants
Study completion date: December 1, 2024
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
January 1, 2021
Actual (reported)
Primary Completion
December 1, 2024
Actual (reported)
Study Completion
December 1, 2024
Actual (reported)
First Submitted
August 19, 2025
Actual (reported)
First Posted
September 12, 2025
Actual (reported)

Last Updated: September 12, 2025
Status Verified: September 2025
Last Update Submitted: September 9, 2025

Conditions

Pain Management

Outcome Measures

Primary Outcomes (1)

pain scores
we will registered the visual analogue scale number
admission at PACU admission, discharge from PACU, 24 hours after surgery (T2)

Eligibility Criteria

Age18 Years+

Sexfemale(Gender-based eligibility)

Healthy VolunteersNo

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodNon-Probability Sample

Study Population

patients with gynaecological malignant or benign condition needed for hysterectomy

You may qualify if:

patients scheduled for robotic hysterectomy acceptation of written informed consent

Sponsors & Collaborators

Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Otherlead
Azienda Ospedaliero Universitaria, Santa Maria della Misericordia di Udine, Italy
Othercollaborator

Study Sites (1)

Fondazione Policlinico Universitario Policlinico Gemelli

Roma, RM, 00166, Italy

Related Publications (1)

Russo A, Perelli F, Aceto P, Arcieri M, Bernardini F, Pregnolato S, Moroni R, Dogareschi T, Meroi F, Costantini B, Gallotta V, Fanfani F, Driul L, Fagotti A, Bove T, Restaino S, Antonelli M, Vizzielli G. Intrathecal morphine dose optimization in robotic-assisted laparoscopic hysterectomy: a dual-center cohort study. J Robot Surg. 2026 May 12;20(1):481. doi: 10.1007/s11701-026-03445-y.
PMID: 42115438DERIVED

MeSH Terms

Conditions

Agnosia

Condition Hierarchy (Ancestors)

Perceptual DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Enrollment

100 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: OTHER
Time Perspective: RETROSPECTIVE
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: medical doctor

Study Record Dates

First Submitted

August 19, 2025

First Posted

September 12, 2025

Study Start

January 1, 2021

Actual (reported)

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You may not qualify if:

were contraindications to neuraxial anesthesia (such as coagulopathies, platelet count below 100,000/mm³ or thrombocytopathy), severe valvular heart disease, left ventricular ejection fraction less than 35%, history of obstructive or restrictive pulmonary disease, or significant neurological disorders

Contact the study team to confirm eligibility.

Primary Completion

December 1, 2024

Actual (reported)

Study Completion

December 1, 2024

Actual (reported)

Last Updated

September 12, 2025

Record last verified: 2025-09

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT07169604
Data provider: ClinicalTrials.gov
Source updated: 2025-09-12
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:21:12 UTC

Locations

IT(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

Primary Completion

Study Completion

First Submitted

First Posted

Conditions

Outcome Measures

Primary Outcomes (1)

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

Related Publications (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations