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CompletedNCT01080313LORHANUpdated Feb 13, 2012

Head and Neck Cancer Registry (LORHAN)

An observational study in Head and Neck Cancer, sponsored by Eli Lilly and Company. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2012-02-13.

Sponsored by Eli Lilly and Company · Observational

Study type
Observational
Time perspective
Prospective
Enrollment
26,000
Ages
18 Years and older
Sex
All
01

Study summary

The primary objective of this study is to describe, in detail, patterns of care for head and neck carcinoma patient

02

Conditions studied

  • Head and Neck Cancer
03

In context

Head and Neck Neoplasms

2,344 studies on the registry are indexed under Head and Neck Neoplasms; 551 are open to participants now.

This study's planned enrollment of 26,000 is above the median of 100 across 441 observational studies indexed under Head and Neck Neoplasms.

Browse Head and Neck Neoplasms studies →

Lead sponsor

Eli Lilly and Company is the lead sponsor of 2,048 studies on the registry; 140 are open to participants now.

Of its 521 completed or terminated interventional studies of FDA-regulated products, 341 (65%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Primary care clinic

Inclusion criteria

  • Pathologically (histologically or cytologically) confirmed new diagnosis of carcinoma involving the oral cavity, oropharynx, nasopharynx, hypopharynx, larynx, or neck node metastasis from unknown origin
  • Scheduled to receive radiotherapy and/or drug therapy including chemotherapy, biologic therapy and targeted therapy
  • Written informed consent

Exclusion criteria

Exclusion Criteria:

  • Registry participation does not exclude participation in clinical trials.
  • Patients scheduled to receive or who have received surgery are eligible for Registry participation as long as they are also scheduled to receive medical therapy.
05

Study design

Time perspective
Prospective
Enrollment
26,000 participants (estimated)

Groups and cohorts

  • Patients with head and neck cancer

    Other: Therapy for head and neck cancer

Interventions

  • OtherTherapy for head and neck cancer

    radiotherapy and/or drug therapy including chemotherapy, biologic therapy and targeted therapy

06

What researchers measure

Primary outcomes

  1. Patterns of care for head and neck cancer

    Time frame: up to 10 years

Secondary outcomes

  1. Overall survival by treatment regimen

    Time frame: study entry to death from any cause or to end of study

  2. Determine the incidence and severity of major dose-limiting and other important treatment toxicities

    Time frame: up to 10 years

  3. Identify supportive care received for managing nutrition, pain, nausea and other complications

    Time frame: up to 10 years

  4. tumor control by treatment regimen

    Time frame: study entry to progressive disease

07

Study locations

1 site
  • Mednet Solutions
    Minnetonka, Minnesota 55305, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 13, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01080313
Lead sponsor
Eli Lilly and Company
Responsible party
Sponsor
First posted
Mar 4, 2010
Start date
Aug 2005
Primary completion
Dec 2011
Completion
Dec 2011
Last update
Feb 13, 2012

Study contacts

Mednet Solutions
study director · MedNet Solutions

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2012. You cannot join it, but the record below documents what was studied.

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