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OpenTrials
Completed

NCT Number: NCT03307525

Pain After Breast Surgery

This is a pilot observational study assessing various predictors for acute pain and persistent pain following breast surgery for cancer.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • English speaking undergoing elective breast cancer surgery

Exclusion criteria

  • Patients with recurrent cancer, metastasis, and previous breast surgery

Treatment and study plan

Primary outcomes

  1. Acute Pain

    Time frame: 72 hours after surgery

    Maximum pain score reported postoperatively

Secondary outcomes

  1. Persistent Pain

    Time frame: More than 6 months after surgery

    pain score ≥ 3 or pain that impacts daily life as indicated by a score >0 on any of the 7 daily activity questions more than 6 months after surgery

Sponsors and collaborators

Lead sponsor

Duke University

Other

Collaborators

  • Society for Ambulatory Anesthesia (SAMBA)

Registry information

Official study title

A Pilot Study Assessing the Correlation of Preoperative Sensory Testing and Genetic Polymorphisms With Acute and Persistent Postoperative Pain

Important dates

Study start
2012
Primary completion
2015
Study completion
2015
First posted
Oct 11, 2017
Registry last updated
Oct 26, 2023

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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