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Same-day Versus Separate-day Preoperative Consultation for Mohs Surgery

Same-day Versus Separate-day Preoperative Consultation for Mohs Surgery

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02321982
Enrollment
0
Registered
2014-12-22
Start date
2015-02-28
Completion date
2017-06-29
Last updated
2017-07-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Basal Cell Carcinoma, Non-melanoma Skin Cancer, Squamous Cell Carcinoma of Skin

Keywords

Mohs surgery, Preoperative consultation

Brief summary

The purpose of this study is to determine whether separate- versus same-day preoperative consultation affects time to treatment (start to finish), utilization rate of Mohs, rate of case cancellations, cost, and patient satisfaction. The investigators hypothesize that patients with same-day preoperative consultation will have a shorter time between cancer diagnosis and removal but, only when coordination of care is needed, longer time between removal and consultation with other specialists, as compared to patients with separate-day consultation. The investigators anticipate that patients with same-day preoperative consultation will have a decrease in travel cost as compared to patients with separate-day consultation. The investigators expect that there will be no difference in various satisfaction matters between groups, with the exception of potentially greater convenience reported by patients in the same-day preoperative consultation group. Finally, the investigators hypothesize that there will be no difference between groups in regards to rates of surgery cancellation.

Detailed description

Procedure: Prospective trial which randomly assigns patients to either separate- or same-day preoperative consultation for Mohs surgery. A phone consultation will take place, which will assist in determining whether the patient is appropriate for enrollment into the study. If so, the patient will be randomized to either separate-day or same-day preoperative consultation. Materials: Patient survey Methods of data collection: The patient-specific data obtained from the medical record will include: Patient age, number of previous skin cancers, preoperative size, history of cutaneous surgery, employment status, and distance between home address and dermatology facility. Outcome measures that will be obtained from the medical record will include: Time between cancer diagnosis, removal and defect repair, rate of proceeding with Mohs as opposed to other treatment options, and rate of cancelling surgery (due to site discrepancy, anticoagulation issues). A survey will be used to assess patient satisfaction.

Interventions

OTHERSame-day preoperative consultation

Preoperative consultation occurs on the same day as Mohs surgery

Sponsors

Dartmouth-Hitchcock Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patients will be considered for enrollment if they have been referred to a Mohs surgeon for consideration of Mohs surgery for non-melanoma skin cancer

Exclusion criteria

* Patients would be excluded if there is a lack of indication for Mohs * Significant comorbidities, or * In the case of a high-risk location or tumor size, for which in advance it is known that they will need consultation with other specialties

Design outcomes

Primary

MeasureTime frameDescription
Time to treatmentEight weeksAssess the total amount of time elapsed between skin cancer diagnosis and defect repair
Time to consultation with other specialtiesEight weeksAssess the amount of time between cancer diagnosis and consultation with non-dermatologic specialties
Time to repairEight weeksAssess the amount of time elapsed between cancer removal and defect repair
Patient satisfactionEight weeksAdminister a survey to assess patient's perception of convenience, level of comfort with the procedure, and self-evaluation of knowledge regarding the diagnosis and treatment

Secondary

MeasureTime frameDescription
Rate of case cancellationEight weeksAssess the number of cases that are cancelled due to site discrepancy, anticoagulation or other medical issues in each arm
Travel costEight weeksAssess the total distance traveled by each patient coming and going to Mohs appointment(s)
Utilization rate of Mohs surgeryEight weeksAssess the percentage of patients who actually proceed with undergoing Mohs surgery in each arm

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026