NCT01535963

Brief Summary

The primary objective of this study is to measure the overall level of satisfaction in patients after cutaneous surgery in 4 different categories, including the surgeon, facility, procedure and recovery and outcome.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
354

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jun 2012

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 7, 2012

Completed
13 days until next milestone

First Posted

Study publicly available on registry

February 20, 2012

Completed
3 months until next milestone

Study Start

First participant enrolled

June 1, 2012

Completed
13.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2025

Completed
Last Updated

January 31, 2025

Status Verified

January 1, 2025

Enrollment Period

13.5 years

First QC Date

February 7, 2012

Last Update Submit

January 29, 2025

Conditions

Skin Cancer

Outcome Measures

Primary Outcomes (1)

  • Patient rating

    Subjects will rate their satisfaction after cutaneous surgery in 4 different categories using 0-10 visual analog scales. The scale will be \~100 millimeters in length and each response will be given a value in millimeters. In addition, patients will answer an open-ended question about their level of satisfaction. Data will also be compared to previous data from patients after cutaneous surgery in the literature.

    at time of visit

Secondary Outcomes (1)

  • Patient ranking

    at time of visit

Study Arms (1)

cutaneous surgery

Patients undergoing cutaneous surgery

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients undergoing cutaneous surgery

You may qualify if:

  • years old
  • Is in a self-reported stable health condition
  • English speaking
  • Is willing and has the ability to understand the study, provide informed consent and communicate with the investigator
  • Recommended to have and scheduled for cutaneous surgery
  • Agrees to follow-up at scheduled times

You may not qualify if:

  • Unable to speak or read English
  • Did not complete an 8th grade education
  • A history of mental illness
  • Any other disability or condition that would prevent completion of questionnaire

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Northwestern University Feinberg School of Medicine, Department of Dermatology

Chicago, Illinois, 60611, United States

Location

MeSH Terms

Conditions

Skin Neoplasms

Condition Hierarchy (Ancestors)

Neoplasms by SiteNeoplasmsSkin DiseasesSkin and Connective Tissue Diseases

Study Officials

  • Murad Alam, MD

    Northwestern University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor in Dermatology, Otolaryngology - Head and Neck Surgery, and Surgery-Organ Transplantation

Study Record Dates

First Submitted

February 7, 2012

First Posted

February 20, 2012

Study Start

June 1, 2012

Primary Completion

December 1, 2025

Study Completion

December 1, 2025

Last Updated

January 31, 2025

Record last verified: 2025-01

Locations

US(1)